Quinolin-2-one derivatives

ABSTRACT

Compounds of the formula I 
     
       
         
         
             
             
         
       
     
     in which X 1 , X 2 , X 3 , X 4 , R 1 , R 2 , R 3 , Q and Y have the meanings indicated in Claim 1,
 
are inhibitors of c-Kit kinase, and can be employed for the treatment of cancer.

BACKGROUND OF THE INVENTION

The invention had the object of finding novel compounds having valuableproperties, in particular those which can be used for the preparation ofmedicaments.

The present invention relates to quinolin-2-one derivatives whichinhibit c-KIT kinase across a wide range of c-KIT mutations andsecondary mutations (V654A secondary resistance mutation in Exon 13)that may arise in GIST (gastrointestinal stromal tumor) patients.

The compounds of this invention are therefore useful in treatingdiseases such as cancer.

The present invention also provides methods for preparing thesecompounds, pharmaceutical compositions comprising these compounds, thecompounds for use for the treatment of diseases and methods of treatingdiseases utilizing pharmaceutical compositions comprising thesecompounds.

Mutated forms of the receptor tyrosine kinase c-KIT are “drivers” inseveral cancers and are attractive targets for therapy. While benefitshave been obtained from use of inhibitors of KIT kinase activity such asimatinib, especially in GIST, primary resistance occurs with certainoncogenic mutations.

Furthermore, resistance frequently develops due to secondary mutations(L. K. Ashman & R. Griffith (2013) Expert Opinion on InvestigationalDrugs, 22:1, 103-115).

L. L. Chen et al. describe “A Missense Mutation in KIT kinase domain 1correlates with imatinib resistance in gastrointestinal stromal tumors”in Cancer res. 2004; 64:5913-5919.

K. G. Roberts et al. describe “Resistance to c-KIT kinase inhibitorsconferred by V654A mutation” in Mol. Cancer Ther. 2007; 6:1159-1166.

Gastrointestinal stromal tumors (GISTs) are the most common mesenchymaltumors of the gastrointestinal (GI) tract.

GISTs are defined as c-KIT (CD117, stem cell factor receptor)-positivemesenchymal spindle cell or epitheloid neoplasms.

GISTs have commonly primary activating mutations of the KIT gene (90%)leading to ligand-independent activation of the receptor tyrosine kinasec-KIT rendering the tumor dependent on oncogenic KIT activity.

Imatinib treatment of GISTs with primary mutation has an initialresponse rate of ˜70% but secondary resistance emerges in almost alltumors.

Approximately 60-70% of patients failing on Imatinib harbor thesecondary V654A resistance mutation in c-KIT.

There is a high unmet medical need for development of a safe andspecific inhibitor against KIT V654A resistance mutation.

It has been found that the compounds according to the invention andsalts thereof have very valuable pharmacological properties while beingwell tol-erated.

The present invention specifically relates to compounds of the formula Iwhich inhibit c-KIT kinase, preferably the mutant V654A of c-KIT kinase.

Moreover, compounds of the formula I inhibit PDGFRα(V651D). Thegain-of-function mutations of PDGFRα appear to play an important role indevelopment of GISTs without KIT mutations (S. Hirota et al.,Gastroenterology 2003; 125:660-667).

The host or patient can belong to any mammalian species, for example aprimate species, particularly humans; rodents, including mice, rats andhamsters; rabbits; horses, cows, dogs, cats, etc. Animal models are ofinterest for experimental investigations, providing a model fortreatment of human disease.

The susceptibility of a particular cell to treatment with the compoundsaccording to the invention can be determined by in vitro tests.Typically, a culture of the cell is combined with a compound accordingto the invention at various concentrations for a period of time which issufficient to allow active agents such as anti IgM to induce a cellularresponse such as expression of a surface marker, usually between aboutone hour and one week. In vitro testing can be carried out usingcultivated cells from blood or from a biopsy sample. The amount ofsurface marker expressed is assessed by flow cytometry using specificantibodies recognising the marker.

The dose varies depending on the specific compound used, the specificdisease, the patient status, etc. A therapeutic dose is typicallysufficient considerably to reduce the undesired cell population in thetarget tissue while the viability of the patient is maintained. Thetreatment is generally continued until a considerable reduction hasoccurred, for example an at least about 50% reduction in the cellburden, and may be continued until essentially no more undesired cellsare detected in the body.

PRIOR ART

-   T. N. Glasnov and C. O. Kappe describe in QSAR Comb. Sci 2007, 26,    1261 the compound-   6,7-dimethoxy-3-(1-phenyl-1H-1,2,3-triazol-4-yl)quinolin-2(1H)-one

having fluorescent characteristics.

Dihydronaphthyridines and related compounds are described in WO2013/184119 A1 as inhibitors of c-Kit mutants including the V654Amutant.

SUMMARY OF THE INVENTION

The invention relates to compounds of the formula I

in which

-   X¹, X², X³, X⁴ each, independently of one another, denote CH or N,-   Y denotes N or CH,-   Q denotes H or CH₃,-   R¹ denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃,-   R² denotes H, F or Cl,-   R³ denotes phenyl, naphthyl, pyridyl, pyrimidinyl, quinolinyl,    isoquinolinyl, indolyl, indazolyl, thiophenyl, dihydroisoindolyl or    benzimidazolyl, each of which is unsubstituted or mono-, di- or    trisubstituted by Hal, CN, NO₂, A, (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂,    (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)COHet,    (CR⁴)_(n)SO₂N(R⁴)₂, (CR⁴)_(n)SO₂Het, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)Het,    O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het, (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het,    (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂,    (CR⁴)_(n)N(R⁴)COA, (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or    (CR⁴)_(n)COOR⁴,-   R⁴ denotes H or A′,-   A denotes unbranched or branched alkyl with 1-10 C-atoms, wherein    two adjacent carbon atoms may form a double bond and/or one or two    non-adjacent CH- and/or CH₂-groups may be replaced by N-, O- and/or    S-atoms and wherein 1-7H-atoms may be replaced by R⁵,    -   or cyclic alkyl having 3-7 C atoms,-   A′ denotes unbranched or branched alkyl with 1-6 C-atoms, wherein    one or two non-adjacent CH- and/or CH₂-groups may be replaced by    O-atoms,-   Cyc denotes cyclobutyl, cyclopentyl or cyclohexyl, each of which is    unsubstituted or mono- or disubstituted by A, Hal, OR⁴, N(R⁴)₂,    Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂ and/or ═O,-   R⁵ denotes F, Cl or OH,-   Het denotes pyrrolidinyl, morpholinyl, piperidinyl, piperazinyl,    [1,4]-diazepanyl, oxazolidinyl, hexahydro-pyrrolo[3,4-c]pyrrolyl,    2-oxa-6-aza-spiro[3.4]octanyl, 2-oxa-6-aza-spiro[3.5]nonanyl,    2-oxa-7-aza-spiro[3.5]nonanyl, 2,5-dioxa-8-aza-spiro[3.5]nonanyl,    oxetanyl, 2-oxa-5-aza-spiro[3.4]octanyl,    2-oxa-6-aza-spiro[3.3]heptanyl, 3-aza-bicyclo[3.1.0]hexanyl,    2-oxa-7-aza-spiro[3.5]nonanyl, isoxazolidinyl, azetidinyl,    2,6-diaza-spiro[3.4]octanyl, hexahydro-pyrrolo[3,4-b]pyrrolyl,    tetrahydrofuranyl or isothiazolidinyl, each of which is    unsubstituted or mono-, di- or trisubstituted by A, Hal, OR⁴, OCOA,    COA, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′,    CON(R⁴)₂, COHet′, (CR⁴)_(n)S(O)_(m)R⁴, and/or ═O,-   Het′ denotes pyrrolidinyl, morpholinyl, piperidinyl, oxetanyl,    tetrahydrofuranyl, tetrahydropyranyl, pyridyl, pyrazolyl or    piperazinyl, each of which is unsubstituted or mono- or    disubstituted by A, Hal, OR⁴, N(R⁴)₂ and/or ═O,-   Hal denotes F, Cl, Br or I,-   n denotes 0, 1, 2 or 3,-   m denotes 0, 1 or 2,

with the proviso that only one or two of X¹, X², X³, X⁴ denote N, andpharmaceutically acceptable salts, tautomers and stereoisomers thereof,including mixtures thereof in all ratios.

The invention also relates to the optically active forms(stereoisomers), the enantiomers, the racemates, the diastereomers andthe hydrates and solvates of these compounds.

Moreover, the invention relates to pharmaceutically acceptablederivatives of compounds of formula I.

The term solvates of the compounds is taken to mean adductions of inertsolvent molecules onto the compounds which form owing to their mutualattractive force. Solvates are, for example, mono- or dihydrates oralkoxides. It is understood, that the invention also relates to thesolvates of the salts. The term pharmaceutically acceptable derivativesis taken to mean, for example, the salts of the compounds according tothe invention and also so-called prodrug compounds.

As used herein and unless otherwise indicated, the term “prodrug” meansa derivative of a compound of formula I that can hydrolyze, oxidize, orotherwise react under biological conditions (in vitro or in vivo) toprovide an active compound, particularly a compound of formula I.Examples of prodrugs include, but are not limited to, derivatives andmetabolites of a compound of formula I that include biohydrolyzablemoieties such as biohydrolyzable amides, biohydrolyzable esters,biohydrolyzable carbamates, biohydrolyzable carbonates, biohydrolyzableureides, and biohydrolyzable phosphate analogues.

In certain embodiments, prodrugs of compounds with carboxyl functionalgroups are the lower alkyl esters of the carboxylic acid. Thecarboxylate esters are conveniently formed by esterifying any of thecarboxylic acid moieties present on the molecule. Prodrugs can typicallybe prepared using well-known methods, such as those described byBurger's Medicinal Chemistry and Drug Discovery 6th ed. (Donald J.Abraham ed., 2001, Wiley) and Design and Application of Prodrugs (H.Bundgaard ed., 1985, Harwood Academic Publishers Gmfh).

The expression “effective amount” denotes the amount of a medicament orof a pharmaceutical active ingredient which causes in a tissue, system,animal or human a biological or medical response which is sought ordesired, for example, by a researcher or physician.

In addition, the expression “therapeutically effective amount” denotesan amount which, compared with a corresponding subject who has notreceived this amount, has the following consequence:

improved treatment, healing, prevention or elimination of a disease,syn-drome, condition, complaint, disorder or side-effects or also thereduction in the advance of a disease, complaint or disorder.

The expression “therapeutically effective amount” also encompasses theamounts which are effective for increasing normal physiologicalfunction.

The invention also relates to the use of mixtures of the compounds ofthe formula I, for example mixtures of two diastereomers, for example inthe ratio 1:1, 1:2, 1:3, 1:4, 1:5, 1:10, 1:100 or 1:1000.

These are particularly preferably mixtures of stereoisomeric compounds.

“Tautomers” refers to isomeric forms of a compound that are inequilibrium with each other. The concentrations of the isomeric formswill depend on the environment the compound is found in and may bedifferent depending upon, for example, whether the compound is a solidor is in an organic or aqueous solution.

The invention relates to the compounds of the formula I and saltsthereof and to a process for the preparation of compounds of the formulaI and pharmaceutically acceptable salts, solvates, tautomers andstereoisomers thereof, characterised in that

a) for the preparation of compounds of the formula I,

wherein

X¹, X², X³, X⁴ denote CH and

Y denotes N,

a compound of the formula II

in which R¹, R² and Q have the meanings indicated in Claim 1,

is reacted with a compound of formula III

N₃—R³  III

in which R³ has the meanings indicated in Claim 1,

or

b) for the preparation of compounds of the formula I,

wherein

Y denotes N,

a compound of the formula IV

in which

and X¹, X², X³, X⁴, R¹, R² and Q have the meanings indicated in Claim 1,

is reacted with a compound of formula V

in which R³ has the meanings indicated in Claim 1,

or

c) a radical R³ is converted into another radical R³ by

-   -   i) converting a carboxylic group into an amide,    -   ii) acylating or alkylating an amino group,

or

d) that a compound of formula I is liberated from one of its functionalderivatives by treatment with a solvolysing or hydrogenolysing agent,

and/or

a base or acid of the formula I is converted into one of its salts.

Above and below, the radicals X¹, X², X³, X⁴, R¹, R², R³, Q and Y havethe meanings indicated for the formula I, unless explicitely statedotherwise.

A denotes alkyl, this is unbranched (linear) or branched, and has 1, 2,3, 4, 5, 6, 7, 8, 9 or 10 C atoms. A preferably denotes methyl, ethyl,propyl, isopropyl, butyl, isobutyl, sec-butyl or tert-butyl, furthermorealso pentyl, 1-, 2- or 3-methylbutyl, 1,1-, 1,2- or 2,2-dimethylpropyl,1-ethylpropyl, hexyl, 1-, 2-, 3- or 4-methylpentyl, 1,1-, 1,2-, 1,3-,2,2-, 2,3- or 3,3-dimethylbutyl, 1- or 2-ethylbutyl,1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, 1,1,2- or1,2,2-trimethylpropyl, furthermore preferably, for example,trifluoromethyl. A very particularly preferably denotes alkyl having 1,2, 3, 4, 5 or 6 C atoms, preferably methyl, ethyl, propyl, isopropyl,butyl, isobutyl, sec-butyl, tert-butyl, pentyl, hexyl, trifluoromethyl,pentafluoroethyl or 1,1,1-trifluoroethyl. Cyclic alkyl preferablydenotes cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.

Moreover, A denotes preferably CH₂OCH₃, CH₂CH₂OH or CH₂CH₂OCH₃.

A′ denotes alkyl, this is unbranched (linear) or branched, and has 1, 2,3, 4, 5 or 4 6 atoms. A′ preferably denotes methyl, ethyl, propyl,isopropyl, butyl, isobutyl, sec-butyl or tert-butyl. Moreover, A′denotes preferably CH₂OCH₃, CH₂CH₂OH or CH₂CH₂OCH₃.

R¹ preferably denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃; particularlypreferably F or Cl.

R² preferably denotes H or F; particularly preferably F.

R³ preferably denotes phenyl, pyridyl, pyrimidinyl, indolyl, indazolyl,thiophenyl, dihydroisoindolyl or benzimidazolyl, each of which isunsubstituted or mono-, di- or trisubstituted by Hal, A, (CR⁴)_(n)OR⁴,(CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)COHet,(CR⁴)_(n)SO₂Het, (CR⁴)_(n)Het, O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het,(CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het,(CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)N(R⁴)COA,(CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or (CR⁴)_(n)COOR⁴.

R³ more preferably denotes phenyl, which is unsubstituted or mono-, di-or trisubstituted by Hal, A, (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂,(CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)COHet, (CR⁴)_(n)SO₂Het,(CR⁴)_(n)Het, O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het,(CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het,(CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)N(R⁴)COA,(CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or (CR⁴)_(n)COOR⁴;

A preferably denotes unbranched or branched alkyl with 1-10 C-atoms,wherein two adjacent carbon atoms may form a double bond and/or one ortwo non-adjacent CH- and/or CH₂-groups may be replaced by N- and/orO-atoms and wherein 1-7H-atoms may be replaced by R⁵.

Het′ preferably denotes pyrrolidinyl.

X¹, X², X³, X⁴ preferably denote CH.

Y preferably denotes N.

Throughout the invention, all radicals which occur more than once may beidentical or different, i.e. are independent of one another.

The compounds of the formula I may have one or more chiral centres andcan therefore occur in various stereoisomeric forms. The formula Iencompasses all these forms.

Accordingly, the invention relates, in particular, to the compounds ofthe formula I in which at least one of the said radicals has one of thepreferred meanings indicated above. Some preferred groups of compoundsmay be expressed by the following sub-formulae Ia to If, which conformto the formula I and in which the radicals not designated in greaterdetail have the meaning indicated for the formula I, but in which

-   in Ia R¹ denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃,    -   R² denotes H or F;-   in Ib R³ denotes phenyl, pyridyl, pyrimidinyl, indolyl, indazolyl,    thiophenyl, dihydroisoindolyl or benzimidazolyl, each of which is    unsubstituted or mono-, di- or trisubstituted by Hal, A,    (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴,    (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)COHet, (CR⁴)_(n)SO₂Het, (CR⁴)_(n)Het,    O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het, (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het,    (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂,    (CR⁴)_(n)N(R⁴)COA, (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or    (CR⁴)_(n)COOR⁴;-   in Ic A denotes unbranched or branched alkyl with 1-10 C-atoms,    wherein two adjacent carbon atoms may form a double bond and/or one    or two non-adjacent CH- and/or CH₂-groups may be replaced by N-    and/or O-atoms and wherein 1-7H-atoms may be replaced by R⁵;-   in Id Het′ denotes pyrrolidinyl;-   in Ie X¹, X², X³, X⁴ each, independently of one another, denote CH    or N,    -   Y denotes N or CH,    -   Q denotes H or CH₃,    -   R¹ denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃,    -   R² denotes H or F,    -   R³ denotes phenyl, pyridyl, pyrimidinyl, indolyl, indazolyl,        thiophenyl, dihydroisoindolyl or benzimidazolyl, each of which        is unsubstituted or mono-, di- or trisubstituted by Hal, A,        (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴,        (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)COHet, (CR⁴)_(n)SO₂Het,        (CR⁴)_(n)Het, O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het,        (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het,        (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)N(R⁴)COA,        (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or (CR⁴)_(n)COOR⁴,    -   R⁴ denotes H or A′,    -   A denotes unbranched or branched alkyl with 1-10 C-atoms,        wherein two adjacent carbon atoms may form a double bond and/or        one or two non-adjacent CH- and/or CH₂-groups may be replaced by        N- and/or O-atoms and wherein 1-7H-atoms may be replaced by R⁵,    -   Cyc denotes cyclobutyl, cyclopentyl or cyclohexyl, each of which        is unsubstituted or mono- or disubstituted by A, Hal, OR⁴,        N(R⁴)₂, Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂ and/or ═O,    -   A′ denotes unbranched or branched alkyl with 1-6 C-atoms,        wherein one or two non-adjacent CH- and/or CH₂-groups may be        replaced by O-atoms,    -   R⁵ denotes F, Cl or OH,    -   Het denotes pyrrolidinyl, morpholinyl, piperidinyl, piperazinyl,        [1,4]-diazepanyl, oxazolidinyl,        hexahydro-pyrrolo[3,4-c]pyrrolyl, 2-oxa-6-aza-spiro[3.4]octanyl,        2-oxa-6-aza-spiro[3.5]nonanyl, 2-oxa-7-aza-spiro[3.5]nonanyl,        2,5-dioxa-8-aza-spiro[3.5]nonanyl, oxetanyl,        2-oxa-5-aza-spiro[3.4]octanyl, 2-oxa-6-aza-spiro[3.3]heptanyl,        3-aza-bicyclo[3.1.0]hexanyl, 2-oxa-7-aza-spiro[3.5]nonanyl,        isoxazolidinyl, azetidinyl, 2,6-diaza-spiro[3.4]octanyl,        hexahydro-pyrrolo[3,4-b]pyrrolyl, tetrahydrofuranyl or        isothiazolidinyl, each of which is unsubstituted or mono-, di-        or trisubstituted by A, Hal, OR⁴, OCOA, COA, (CR⁴)_(n)N(R⁴)₂,        (CR⁴)_(n)Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂, COHet′,        (CR⁴)_(n)S(O)_(m)R⁴, and/or ═O,    -   Het′ denotes pyrrolidinyl, oxetanyl, tetrahydrofuranyl,        tetrahydropyranyl, pyridyl or pyrazolyl,    -   Hal denotes F, Cl, Br or I,    -   n denotes 0, 1, 2 or 3,    -   m denotes 0, 1 or 2,-   in If X¹, X², X³, X⁴ denote CH,    -   Y denotes N,    -   Q denotes H or CH₃,    -   R¹ denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃,    -   R² denotes H or F,    -   R³ denotes phenyl, which is unsubstituted or mono-, di- or        trisubstituted by Hal, A, (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂,        (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)_(n)CON(R⁴)₂, (CR⁴)_(n)OCOHet,        (CR⁴)_(n)SO₂Het, (CR⁴)_(n)Het, O(CR⁴)_(n)COHet,        (CR⁴)_(n)O(CR⁴)_(n)Het, (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het,        (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂,        (CR⁴)_(n)N(R⁴)COA, (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or        (CR⁴)_(n)COOR⁴,    -   R⁴ denotes H or A′,    -   A denotes unbranched or branched alkyl with 1-10 C-atoms,        wherein two adjacent carbon atoms may form a double bond and/or        one or two non-adjacent CH- and/or CH₂-groups may be replaced by        N- and/or O-atoms and wherein 1-7H-atoms may be replaced by R⁵,    -   Cyc denotes cyclobutyl, cyclopentyl or cyclohexyl, each of which        is unsubstituted or mono- or disubstituted by A, Hal, OR⁴,        N(R⁴)₂, Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂ and/or ═O,    -   A′ denotes unbranched or branched alkyl with 1-6 C-atoms,        wherein one or two non-adjacent CH- and/or CH₂-groups may be        replaced by O-atoms,    -   R⁵ denotes F, Cl or OH,    -   Het denotes pyrrolidinyl, morpholinyl, piperidinyl, piperazinyl,        [1,4]-diazepanyl, oxazolidinyl,        hexahydro-pyrrolo[3,4-c]pyrrolyl, 2-oxa-6-aza-spiro[3.4]octanyl,        2-oxa-6-aza-spiro[3.5]nonanyl, 2-oxa-7-aza-spiro[3.5]nonanyl,        2,5-dioxa-8-aza-spiro[3.5]nonanyl, oxetanyl,        2-oxa-5-aza-spiro[3.4]octanyl, 2-oxa-6-aza-spiro[3.3]heptanyl,        3-aza-bicyclo[3.1.0]hexanyl, 2-oxa-7-aza-spiro[3.5]nonanyl,        isoxazolidinyl, azetidinyl, 2,6-diaza-spiro[3.4]octanyl,        hexahydro-pyrrolo[3,4-b]pyrrolyl, tetrahydrofuranyl or        isothiazolidinyl, each of which is unsubstituted or mono-, di-        or trisubstituted by A, Hal, OR⁴, OCOA, COA, (CR⁴)_(n)N(R⁴)₂,        (CR⁴)_(n)Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂, COHet′,        (CR⁴)_(n)S(O)_(m)R⁴, and/or ═O,    -   Het′ denotes pyrrolidinyl, oxetanyl, tetrahydrofuranyl,        tetrahydropyranyl, pyridyl or pyrazolyl,    -   Hal denotes F, Cl, Br or I,    -   n denotes 0, 1, 2 or 3,    -   m denotes 0, 1 or 2,

and pharmaceutically acceptable salts, tautomers and stereoisomersthereof, including mixtures thereof in all ratios.

The compounds of the formula I and also the starting materials for theirpreparation are, in addition, prepared by methods known per se, asdescribed in the literature (for example in the standard works, such asHouben-Weyl, Methoden der organischen Chemie [Methods of OrganicChemistry], Georg-Thieme-Verlag, Stuttgart), to be precise underreaction conditions which are known and suitable for the said reactions.Use can also be made here of variants known per se which are notmentioned here in greater detail.

The starting compounds of the formula II and III are generally known. Ifthey are novel, however, they can be prepared by methods known per se.Compounds of the formula I can preferably be obtained by reacting acompound of the formula II with a compound of the formula III. Thereactions is known as “Click-reaction” and is generally carried out inan inert solvent, preferably in the presence of CuSO₄ and sodiumascorbate or isoascorbate.

Depending on the conditions used, the reaction time is between a fewminutes and 14 days, the reaction temperature is between about 0° and140°, normally between 20° and 130°, in particular between about 80° andabout 120°.

Examples of suitable inert solvents are hydrocarbons, such as hexane,petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons,such as trichloroethylene, 1,2-dichloroethane, carbon tetrachloride,chloroform or dichloromethane; alcohols, such as methanol, ethanol,isopropanol, n-propanol, n-butanol or tert-butanol; ethers, such asdiethyl ether, diisopropyl ether, tetrahydrofuran (THF) or dioxane;glycol ethers, such as ethylene glycol monomethyl or monoethyl ether,ethylene glycol dimethyl ether (diglyme); ketones, such as acetone orbutanone; amides, such as acetamide, dimethylacetamide ordimethylformamide (DMF); nitriles, such as acetonitrile; sulfoxides,such as dimethyl sulfoxide (DMSO); carbon disulfide; carboxylic acids,such as formic acid or acetic acid; nitro compounds, such asnitromethane or nitrobenzene; esters, such as ethyl acetate, or mixturesof the said solvents.

Particular preference is given to DMF.

The starting compounds of the formula IV and V are generally known. Ifthey are novel, however, they can be prepared by methods known per se.

Compounds of the formula I can preferably be obtained by reacting acompound of the formula IV with a compound of the formula V.

The reaction is generally carried out in the presence of an acid-bindingagent, preferably an organic base, such as DIPEA, triethylamine,dimethylaniline, pyridine or quinoline.

Moreover, the reaction is generally carried out in the presence of[dimethylamino-([1,2,3]triazolo[4,5-b]pyridin-3-yloxy)-methylene]-dimethyl-ammoniumhexafluorophosphate (HATU).

Depending on the conditions used, the reaction time is between a fewminutes and 14 days, the reaction temperature is between about −30° and140°, normally between −10° and 90°, in particular between about 0° andabout 70°.

Examples of suitable inert solvents are hydrocarbons, such as hexane,petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons,such as trichloroethylene, 1,2-dichloroethane, carbon tetrachloride,chloroform or dichloromethane; alcohols, such as methanol, ethanol,isopropanol, n-propanol, n-butanol or tert-butanol; ethers, such asdiethyl ether, diisopropyl ether, tetrahydrofuran (THF) or dioxane;glycol ethers, such as ethylene glycol monomethyl or monoethyl ether,ethylene glycol dimethyl ether (diglyme); ketones, such as acetone orbutanone; amides, such as acetamide, dimethylacetamide ordimethylformamide (DMF); nitriles, such as acetonitrile; sulfoxides,such as dimethyl sulfoxide (DMSO); carbon disulfide; carboxylic acids,such as formic acid or acetic acid; nitro compounds, such asnitromethane or nitrobenzene; esters, such as ethyl acetate, or mixturesof the said solvents.

Particular preference is given to acetonitrile, dichloromethane and/orDMF. Alternatively, the reaction is carried out under modifiedFrielaender quinolone synthesis conditions, with a carboxylic acidanhydride, such as acetic acid anhydride, as solvent and condensingagent and with an acid binding agent, such as trimethylamine or DIPEA.

It is furthermore possible to convert a compound of the formula I intoanother compound of the formula I, for example by reducing nitro groupsto amino groups (for example by hydrogenation on Raney nickel orPd/carbon in an inert solvent, such as methanol or ethanol).

Free amino groups can furthermore be acylated in a conventional mannerusing an acid chloride or anhydride or alkylated using an unsubstitutedor substituted alkyl halide, advantageously in an inert solvent, such asdichloromethane or THF, and/or in the presence of a base, such astriethylamine or pyridine, at temperatures between −60 and +30°.

The alkylation also can be performed under reducing alkylatingconditions, such as the use of HCHO and NaBH₃CN.

The compounds of the formula I can furthermore be obtained by liberatingthem from their functional derivatives by solvolysis, in particularhydrolysis, or by hydrogenolysis.

Preferred starting materials for the solvolysis or hydrogenolysis arethose which contain corresponding protected amino and/or hydroxyl groupsinstead of one or more free amino and/or hydroxyl groups, preferablythose which carry an aminoprotecting group instead of an H atom bondedto an N atom, for example those which conform to the formula I, butcontain an NHR′ group (in which R′ is an aminoprotecting group, forexample BOC or CBZ) instead of an NH₂ group.

Preference is furthermore given to starting materials which carry ahydroxylprotecting group instead of the H atom of a hydroxyl group, forexample those which conform to the formula I, but contain an R″O-phenylgroup (in which R″ is a hydroxylprotecting group) instead of ahydroxyphenyl group.

It is also possible for a plurality of—identical or different—protectedamino and/or hydroxyl groups to be present in the molecule of thestarting material. If the protecting groups present are different fromone another, they can in many cases be cleaved off selectively.

The term “aminoprotecting group” is known in general terms and relatesto groups which are suitable for protecting (blocking) an amino groupagainst chemical reactions, but are easy to remove after the desiredchemical reaction has been carried out elsewhere in the molecule.Typical of such groups are, in particular, unsubstituted or substitutedacyl, aryl, aralkoxy-methyl or aralkyl groups. Since the aminoprotectinggroups are removed after the desired reaction (or reaction sequence),their type and size are furthermore not crucial; however, preference isgiven to those having 1-20, in particular 1-8, carbon atoms. The term“acyl group” is to be understood in the broadest sense in connectionwith the present process. It includes acyl groups derived fromaliphatic, araliphatic, aromatic or heterocyclic carboxylic acids orsulfonic acids, and, in particular, alkoxycarbonyl, aryloxycarbonyl andespecially aralkoxycarbonyl groups. Examples of such acyl groups arealkanoyl, such as acetyl, propionyl and butyryl; aralkanoyl, such asphenylacetyl; aroyl, such as benzoyl and tolyl; aryloxyalkanoyl, such asPOA; alkoxycarbonyl, such as methoxycarbonyl, ethoxycarbonyl,2,2,2-trichloroethoxycarbonyl, BOC and 2-iodoethoxycarbonyl;aralkoxycarbonyl, such as CBZ (“carbobenzoxy”),4-methoxybenzyloxycarbonyl and FMOC; and arylsulfonyl, such as Mtr, Pbfand Pmc. Preferred aminoprotecting groups are BOC and Mtr, furthermoreCBZ, Fmoc, benzyl and acetyl.

The term “hydroxylprotecting group” is likewise known in general termsand relates to groups which are suitable for protecting a hydroxyl groupagainst chemical reactions, but are easy to remove after the desiredchemical reaction has been carried out elsewhere in the molecule.Typical of such groups are the above-mentioned unsubstituted orsubstituted aryl, aralkyl or acyl groups, furthermore also alkyl groups.The nature and size of the hydroxylprotecting groups are not crucialsince they are removed again after the desired chemical reaction orreaction sequence; preference is given to groups having 1-20, inparticular 1-10, carbon atoms. Examples of hydroxylprotecting groupsare, inter alia, tert-butoxycarbonyl, benzyl, p-nitrobenzoyl,p-toluenesulfonyl, tert-butyl and acetyl, where benzyl and tert-butylare particularly preferred.

The compounds of the formula I are liberated from their functionalderivatives—depending on the protecting group used—for example usingstrong acids, advantageously using TFA or perchloric acid, but alsousing other strong inorganic acids, such as hydrochloric acid orsulfuric acid, strong organic carboxylic acids, such as trichloroaceticacid, or sulfonic acids, such as benzene- or p-toluenesulfonic acid. Thepresence of an additional inert solvent is possible, but is not alwaysnecessary. Suitable inert solvents are preferably organic, for examplecarboxylic acids, such as acetic acid, ethers, such as tetrahydrofuranor dioxane, amides, such as DMF, halogenated hydrocarbons, such asdichloromethane, furthermore also alcohols, such as methanol, ethanol orisopropanol, and water. Mixtures of the above-mentioned solvents arefurthermore suitable. TFA is preferably used in excess without additionof a further solvent, and perchloric acid is preferably used in the formof a mixture of acetic acid and 70% perchloric acid in the ratio 9:1.The reaction temperatures for the cleavage are advantageously betweenabout 0 and about 50°, preferably between 15 and 30° (room temperature).

The BOC, OBut, Pbf, Pmc and Mtr groups can, for example, preferably becleaved off using TFA in dichloromethane or using approximately 3 to 5NHCl in dioxane at 15-30°, and the FMOC group can be cleaved off using anapproximately 5 to 50% solution of dimethylamine, diethylamine orpiperidine in DMF at 15-30°.

Hydrogenolytically removable protecting groups (for example CBZ orbenzyl) can be cleaved off, for example, by treatment with hydrogen inthe presence of a catalyst (for example a noble-metal catalyst, such aspalladium, advantageously on a support, such as carbon). Suitablesolvents here are those indicated above, in particular, for example,alcohols, such as methanol or ethanol, or amides, such as DMF. Thehydrogenolysis is generally carried out at temperatures between about 0and 100° and pressures between about 1 and 200 bar, preferably at 20-30°and 1-10 bar. Hydrogenolysis of the CBZ group succeeds well, forexample, on 5 to 10% Pd/C in methanol or using ammonium formate (insteadof hydrogen) on Pd/C in methanol/DMF at 20-300.

Moreover, compounds of the formula I can preferably be obtained byconverting a radical R³ into another radical R³ by converting acarboxylic group into an amide.

The reaction is generally carried out in the presence of a couplingagent such as HATU and an acid binding agent, preferably an organicbase, such as DIPEA, triethylamine, dimethylaniline, pyridine orquinoline.

The addition of an alkali or alkaline earth metal hydroxide, carbonateor bicarbonate or another salt of a weak acid of the alkali or alkalineearth metals, preferably of potassium, sodium, calcium or caesium, mayalso be favourable.

Depending on the conditions used, the reaction time is between a fewminutes and 14 days, the reaction temperature is between about −30° and140°, normally between −100 and 90°, in particular between about 0° andabout 70°.

Examples of suitable inert solvents are hydrocarbons, such as hexane,petroleum ether, benzene, toluene or xylene; chlorinated hydrocarbons,such as trichloroethylene, 1,2-dichloroethane, carbon tetrachloride,chloroform or dichloromethane; alcohols, such as methanol, ethanol,isopropanol, n-propanol, n-butanol or tert-butanol; ethers, such asdiethyl ether, diisopropyl ether, tetrahydrofuran (THF) or dioxane;glycol ethers, such as ethylene glycol monomethyl or monoethyl ether,ethylene glycol dimethyl ether (diglyme); ketones, such as acetone orbutanone; amides, such as acetamide, dimethylacetamide ordimethylformamide (DMF); nitriles, such as acetonitrile; sulfoxides,such as dimethyl sulfoxide (DMSO); carbon disulfide; carboxylic acids,such as formic acid or acetic acid; nitro compounds, such asnitromethane or nitrobenzene; esters, such as ethyl acetate, or mixturesof the said solvents.

Particular preference is given to acetonitrile, dichloromethane and/orDMF.

Pharmaceutical salts and other forms

The said compounds according to the invention can be used in their finalnon-salt form. On the other hand, the present invention also encompassesthe use of these compounds in the form of their pharmaceuticallyacceptable salts, which can be derived from various organic andinorganic acids and bases by procedures known in the art.Pharmaceutically acceptable salt forms of the compounds of the formula Iare for the most part prepared by conventional methods. If the compoundof the formula I contains a carboxyl group, one of its suitable saltscan be formed by reacting the compound with a suitable base to give thecorresponding base-addition salt. Such bases are, for example, alkalimetal hydroxides, including potassium hydroxide, sodium hydroxide andlithium hydroxide; alkaline earth metal hydroxides, such as bariumhydroxide and calcium hydroxide; alkali metal alkoxides, for examplepotassium ethoxide and sodium propoxide; and various organic bases, suchas piperidine, diethanolamine and N-methylglutamine. The aluminium saltsof the compounds of the formula I are likewise included. In the case ofcertain compounds of the formula I, acid-addition salts can be formed bytreating these compounds with pharmaceutically acceptable organic andinorganic acids, for example hydrogen halides, such as hydrogenchloride, hydrogen bromide or hydrogen iodide, other mineral acids andcorresponding salts thereof, such as sulfate, nitrate or phosphate andthe like, and alkyl- and monoarylsulfonates, such as ethanesulfonate,toluenesulfonate and benzenesulfonate, and other organic acids andcorresponding salts thereof, such as acetate, trifluoroacetate,tartrate, maleate, succinate, citrate, benzoate, salicylate, ascorbateand the like. Accordingly, pharmaceutically acceptable acid-additionsalts of the compounds of the formula I include the following: acetate,adipate, alginate, arginate, aspartate, benzoate, benzenesulfonate(besylate), bisulfate, bisulfite, bromide, butyrate, camphorate,camphorsulfonate, caprylate, chloride, chlorobenzoate, citrate,cyclopentanepropionate, digluconate, dihydrogenphosphate,dinitrobenzoate, dodecylsulfate, ethanesulfonate, fumarate, formate,galacterate (from mucic acid), galacturonate, gluco-heptanoate,gluconate, glutamate, glycerophosphate, hemisuccinate, hemi-sulfate,heptanoate, hexanoate, hippurate, hydrochloride, hydrobromide,hydroiodide, 2-hydroxyethanesulfonate, iodide, isethionate, isobutyrate,lactate, lactobionate, malate, maleate, malonate, mandelate,metaphos-phate, methanesulfonate, methylbenzoate, monohydrogenphosphate,2-naphthalenesulfonate, nicotinate, nitrate, oxalate, oleate, palmoate,pectinate, persulfate, phenylacetate, 3-phenylpropionate, phosphate,phosphonate, phthalate, but this does not represent a restriction.

Furthermore, the base salts of the compounds according to the inventioninclude aluminium, ammonium, calcium, copper, iron(III), iron(II),lithium, magnesium, manganese(III), manganese(II), potassium, sodium andzinc salts, but this is not intended to represent a restriction. Of theabove-mentioned salts, preference is given to ammonium; the alkali metalsalts sodium and potassium, and the alkaline earth metal salts calciumand magnesium. Salts of the compounds of the formula I which are derivedfrom pharmaceutically acceptable organic non-toxic bases include saltsof primary, secondary and tertiary amines, substituted amines, alsoincluding naturally occurring substituted amines, cyclic amines, andbasic ion exchanger resins, for example arginine, betaine, caffeine,chloroprocaine, choline, N,N′-dibenzylethylenediamine (benzathine),dicyclohexylamine, diethanolamine, diethylamine, 2-diethylaminoethanol,2-dimethylaminoethanol, ethanolamine, ethylenediamine,N-ethylmorpholine, N-ethylpiperidine, glucamine, glucosamine, histidine,hydrabamine, isopropylamine, lidocaine, lysine, meglumine,N-methyl-D-glucamine, morpholine, piperazine, piperidine, polyamineresins, procaine, purines, theobromine, triethanolamine, triethylamine,trimethylamine, tripropylamine and tris(hydroxymethyl)methylamine(tromethamine), but this is not intended to represent a restriction.

Compounds of the present invention which contain basicnitrogen-containing groups can be quaternised using agents such as(C₁-C₄)alkyl halides, for example methyl, ethyl, isopropyl andtert-butyl chloride, bromide and iodide; di(C₁-C₄)alkyl sulfates, forexample dimethyl, diethyl and diamyl sulfate; (C₁₀-C₁₈)alkyl halides,for example decyl, dodecyl, lauryl, myristyl and stearyl chloride,bromide and iodide; and aryl(C₁-C₄)alkyl halides, for example benzylchloride and phenethyl bromide. Both water- and oil-soluble compoundsaccording to the invention can be prepared using such salts.

The above-mentioned pharmaceutical salts which are preferred includeacetate, trifluoroacetate, besylate, citrate, fumarate, gluconate,hemisuccinate, hippurate, hydrochloride, hydrobromide, isethionate,mandelate, meglumine, nitrate, oleate, phosphonate, pivalate, sodiumphosphate, stearate, sulfate, sulfosalicylate, tartrate, thiomalate,tosylate and tromethamine, but this is not intended to represent arestriction.

Particular preference is given to hydrochloride, dihydrochloride,hydrobromide, maleate, mesylate, phosphate, sulfate and succinate.

The acid-addition salts of basic compounds of the formula I are preparedby bringing the free base form into contact with a sufficient amount ofthe desired acid, causing the formation of the salt in a conventionalmanner. The free base can be regenerated by bringing the salt form intocontact with a base and isolating the free base in a conventionalmanner. The free base forms differ in a certain respect from thecorresponding salt forms thereof with respect to certain physicalproperties, such as solubility in polar solvents; for the purposes ofthe invention, however, the salts otherwise correspond to the respectivefree base forms thereof.

As mentioned, the pharmaceutically acceptable base-addition salts of thecompounds of the formula I are formed with metals or amines, such asalkali metals and alkaline earth metals or organic amines. Preferredmetals are sodium, potassium, magnesium and calcium. Preferred organicamines are N,N′-dibenzylethylenediamine, chloroprocaine, choline,diethanolamine, ethylenediamine, N-methyl-D-glucamine and procaine.

The base-addition salts of acidic compounds according to the inventionare prepared by bringing the free acid form into contact with asufficient amount of the desired base, causing the formation of the saltin a conventional manner. The free acid can be regenerated by bringingthe salt form into contact with an acid and isolating the free acid in aconventional manner. The free acid forms differ in a certain respectfrom the corresponding salt forms thereof with respect to certainphysical properties, such as solubility in polar solvents; for thepurposes of the invention, however, the salts otherwise correspond tothe respective free acid forms thereof.

If a compound according to the invention contains more than one groupwhich is capable of forming pharmaceutically acceptable salts of thistype, the invention also encompasses multiple salts. Typical multiplesalt forms include, for example, bitartrate, diacetate, difumarate,dimeglumine, di-phosphate, disodium and trihydrochloride, but this isnot intended to represent a restriction.

With regard to that stated above, it can be seen that the expression“pharmaceutically acceptable salt” in the present connection is taken tomean an active ingredient which comprises a compound of the formula I inthe form of one of its salts, in particular if this salt form impartsimproved pharmacokinetic properties on the active ingredient comparedwith the free form of the active ingredient or any other salt form ofthe active ingredient used earlier. The pharmaceutically acceptable saltform of the active ingredient can also provide this active ingredientfor the first time with a desired pharmacokinetic property which it didnot have earlier and can even have a positive influence on thepharmacodynamics of this active ingredient with respect to itstherapeutic efficacy in the body.

Isotopes

There is furthermore intended that a compound of the formula I includesisotope-labelled forms thereof. An isotope-labelled form of a compoundof the formula I is identical to this compound apart from the fact thatone or more atoms of the compound have been replaced by an atom or atomshaving an atomic mass or mass number which differs from the atomic massor mass number of the atom which usually occurs naturally. Examples ofisotopes which are readily commercially available and which can beincorporated into a compound of the formula I by well-known methodsinclude isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus,fluorine and chlorine, for example ²H, ³H, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³¹P,³²p, ³⁵S, ¹⁸F and ³⁶Cl, respectively. A compound of the formula I, aprodrug, thereof or a pharmaceutically acceptable salt of either whichcontains one or more of the above-mentioned isotopes and/or otheriso-topes of other atoms is intended to be part of the presentinvention. An isotope-labelled compound of the formula I can be used ina number of beneficial ways. For example, an isotope-labelled compoundof the formula I into which, for example, a radioisotope, such as ³H or¹⁴C, has been incorporated is suitable for medicament and/or substratetissue distribution assays. These radioisotopes, i.e. tritium (³H) andcarbon-14 (¹⁴C), are particularly preferred owing to simple preparationand excellent detectability. Incorporation of heavier isotopes, forexample deuterium (²H), into a compound of the formula I has therapeuticadvantages owing to the higher metabolic stability of thisisotope-labelled compound. Higher metabolic stability translatesdirectly into an increased in vivo half-life or lower dosages, whichunder most circumstances would represent a preferred embodiment of thepresent invention. An isotope-labelled compound of the formula I canusually be prepared by carrying out the procedures disclosed in thesynthesis schemes and the related description, in the example part andin the preparation part in the present text, replacing anon-isotope-labelled reactant by a readily available isotope-labelledreactant.

Deuterium (²H) can also be incorporated into a compound of the formula Ifor the purpose in order to manipulate the oxidative metabolism of thecompound by way of the primary kinetic isotope effect. The primarykinetic isotope effect is a change of the rate for a chemical reactionthat results from exchange of isotopic nuclei, which in turn is causedby the change in ground state energies necessary for covalent bondformation after this isotopic exchange. Exchange of a heavier isotopeusually results in a lowering of the ground state energy for a chemicalbond and thus cause a reduction in the rate in rate-limiting bondbreakage. If the bond breakage occurs in or in the vicinity of asaddle-point region along the coordinate of a multi-product reaction,the product distribution ratios can be altered substantially. Forexplanation: if deuterium is bonded to a carbon atom at anon-exchangeable position, rate differences of k_(M)/k_(D)=2-7 aretypical. If this rate difference is successfully applied to a compoundof the formula I that is susceptible to oxidation, the profile of thiscompound in vivo can be drastically modified and result in improvedpharmacokinetic properties.

When discovering and developing therapeutic agents, the person skilledin the art attempts to optimise pharmacokinetic parameters whileretaining desirable in vitro properties. It is reasonable to assume thatmany compounds with poor pharmacokinetic profiles are susceptible tooxidative metabolism. In vitro liver microsomal assays currentlyavailable provide valuable information on the course of oxidativemetabolism of this type, which in turn permits the rational design ofdeuterated compounds of the formula I with improved stability throughresistance to such oxidative metabolism. Significant improvements in thepharmacokinetic profiles of compounds of the formula I are therebyobtained, and can be expressed quantitatively in terms of increases inthe in vivo half-life (t1/2), concentration at maximum therapeuticeffect (C_(max)), area under the dose response curve (AUC), and F; andin terms of reduced clearance, dose and materials costs.

The following is intended to illustrate the above: a compound of theformula I which has multiple potential sites of attack for oxidativemetabolism, for example benzylic hydrogen atoms and hydrogen atomsbonded to a nitrogen atom, is prepared as a series of analogues in whichvarious combinations of hydrogen atoms are replaced by deuterium atoms,so that some, most or all of these hydrogen atoms have been replaced bydeuterium atoms. Half-life determinations enable favourable and accuratedetermination of the extent of the extent to which the improvement inresistance to oxidative metabolism has improved. In this way, it isdeter-mined that the half-life of the parent compound can be extended byup to 100% as the result of deuterium-hydrogen exchange of this type.

Deuterium-hydrogen exchange in a compound of the formula I can also beused to achieve a favourable modification of the metabolite spectrum ofthe starting compound in order to diminish or eliminate undesired toxicmetabolites. For example, if a toxic metabolite arises through oxidativecarbon-hydrogen (C—H) bond cleavage, it can reasonably be assumed thatthe deuterated analogue will greatly diminish or eliminate production ofthe unwanted metabolite, even if the particular oxidation is not arate-determining step. Further information on the state of the art withrespect to deuterium-hydrogen exchange may be found, for example inHanzlik et al., J. Org. Chem. 55, 3992-3997, 1990, Reider et al., J.Org. Chem. 52, 3326-3334, 1987, Foster, Adv. Drug Res. 14, 1-40, 1985,Gillette et al, Biochemistry 33(10) 2927-2937, 1994, and Jarman et al.Carcinogenesis 16(4), 683-688, 1993.

The invention furthermore relates to medicaments comprising at least onecompound of the formula I and/or pharmaceutically acceptable salts,solvates and stereoisomers thereof, including mixtures thereof in allratios, and optionally excipients and/or adjuvants.

Pharmaceutical formulations can be administered in the form of dosageunits which comprise a predetermined amount of active ingredient perdosage unit. Such a unit can comprise, for example, 0.5 mg to 1 g,preferably 1 mg to 700 mg, particularly preferably 5 mg to 100 mg, of acompound according to the invention, depending on the condition treated,the method of administration and the age, weight and condition of thepatient, or pharmaceutical formulations can be administered in the formof dosage units which comprise a predetermined amount of activeingredient per dosage unit. Preferred dosage unit formulations are thosewhich comprise a daily dose or part-dose, as indicated above, or acorresponding fraction thereof of an active ingredient. Furthermore,pharmaceutical formulations of this type can be prepared using a processwhich is generally known in the pharmaceutical art.

Pharmaceutical formulations can be adapted for administration via anydesired suitable method, for example by oral (including buccal orsublingual), rectal, nasal, topical (including buccal, sublingual ortransdermal), vaginal or parenteral (including subcutaneous,intramuscular, intravenous or intradermal) methods. Such formulationscan be prepared using all processes known in the pharmaceutical art by,for example, combining the active ingredient with the excipient(s) oradjuvant(s).

Pharmaceutical formulations adapted for oral administration can beadministered as separate units, such as, for example, capsules ortablets; powders or granules; solutions or suspensions in aqueous ornon-aqueous liquids; edible foams or foam foods; or oil-in-water liquidemulsions or water-in-oil liquid emulsions.

Thus, for example, in the case of oral administration in the form of atablet or capsule, the active-ingredient component can be combined withan oral, non-toxic and pharmaceutically acceptable inert excipient, suchas, for example, ethanol, glycerol, water and the like. Powders areprepared by comminuting the compound to a suitable fine size and mixingit with a pharmaceutical excipient comminuted in a similar manner, suchas, for example, an edible carbohydrate, such as, for example, starch ormannitol. A flavour, preservative, dispersant and dye may likewise bepresent.

Capsules are produced by preparing a powder mixture as described aboveand filling shaped gelatine shells therewith. Glidants and lubricants,such as, for example, highly disperse silicic acid, talc, magnesiumstearate, calcium stearate or polyethylene glycol in solid form, can beadded to the powder mixture before the filling operation. A disintegrantor solubiliser, such as, for example, agar-agar, calcium carbonate orsodium carbonate, may likewise be added in order to improve theavailability of the medicament after the capsule has been taken.

In addition, if desired or necessary, suitable binders, lubricants anddisintegrants as well as dyes can likewise be incorporated into themixture. Suitable binders include starch, gelatine, natural sugars, suchas, for example, glucose or beta-lactose, sweeteners made from maize,natural and synthetic rubber, such as, for example, acacia, tragacanthor sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes,and the like. The lubricants used in these dosage forms include sodiumoleate, sodium stearate, magnesium stearate, sodium benzoate, sodiumacetate, sodium chloride and the like. The disintegrants include,without being restricted thereto, starch, methylcellulose, agar,bentonite, xanthan gum and the like. The tablets are formulated by, forexample, preparing a powder mixture, granulating or dry-pressing themixture, adding a lubricant and a disintegrant and pressing the entiremixture to give tablets. A powder mixture is prepared by mixing thecompound comminuted in a suitable manner with a diluent or a base, asdescribed above, and optionally with a binder, such as, for example,carboxymethylcellulose, an alginate, gelatine or polyvinylpyrrolidone, adissolution retardant, such as, for example, paraffin, an ab-sorptionaccelerator, such as, for example, a quaternary salt, and/or anabsorbant, such as, for example, bentonite, kaolin or dicalciumphosphate. The powder mixture can be granulated by wetting it with abinder, such as, for example, syrup, starch paste, acadia mucilage orsolutions of cellulose or polymer materials and pressing it through asieve. As an alternative to granulation, the powder mixture can be runthrough a tabletting machine, giving lumps of non-uniform shape, whichare broken up to form granules. The granules can be lubricated byaddition of stearic acid, a stearate salt, talc or mineral oil in orderto prevent sticking to the tablet casting moulds. The lubricated mixtureis then pressed to give tablets. The compounds according to theinvention can also be combined with a free-flowing inert excipient andthen pressed directly to give tablets without carrying out thegranulation or dry-pressing steps. A transparent or opaque protectivelayer consisting of a shellac sealing layer, a layer of sugar or polymermaterial and a gloss layer of wax may be present. Dyes can be added tothese coatings in order to be able to differentiate between differentdosage units.

Oral liquids, such as, for example, solution, syrups and elixirs, can beprepared in the form of dosage units so that a given quantity comprisesa pre-specified amount of the compound. Syrups can be prepared bydissolving the compound in an aqueous solution with a suitable flavour,while elixirs are prepared using a non-toxic alcoholic vehicle.Suspensions can be formulated by dispersion of the compound in anon-toxic vehicle. Solubilisers and emulsifiers, such as, for example,ethoxylated isostearyl alcohols and polyoxyethylene sorbitol ethers,preservatives, flavour additives, such as, for example, peppermint oilor natural sweeteners or saccharin, or other artificial sweeteners andthe like, can likewise be added.

The dosage unit formulations for oral administration can, if desired, been-capsulated in microcapsules. The formulation can also be prepared insuch a way that the release is extended or retarded, such as, forexample, by coating or embedding of particulate material in polymers,wax and the like.

The compounds of the formula I and pharmaceutically salts, tautomers andstereoisomers thereof can also be administered in the form of liposomedelivery systems, such as, for example, small unilamellar vesicles,large unilamellar vesicles and multilamellar vesicles. Liposomes can beformed from various phospholipids, such as, for example, cholesterol,stearylamine or phosphatidylcholines.

The compounds of the formula I and the salts, tautomers andstereoisomers thereof can also be delivered using monoclonal antibodiesas individual carriers to which the compound molecules are coupled. Thecompounds can also be coupled to soluble polymers as targeted medicamentcarriers. Such polymers may encompass polyvinylpyrrolidone, pyrancopolymer, polyhydroxypropylmethacrylamidophenol,polyhydroxy-ethylaspartamidophenol or polyethylene oxide polylysine,substituted by palmitoyl radicals. The compounds may furthermore becoupled to a class of biodegradable polymers which are suitable forachieving controlled release of a medicament, for example polylacticacid, poly-epsilon-caprolactone, polyhydroxybutyric acid,polyorthoesters, polyacetals, polydihydroxypyrans, polycyanoacrylatesand crosslinked or amphipathic block copolymers of hydrogels.

Pharmaceutical formulations adapted for transdermal administration canbe administered as independent plasters for extended, close contact withthe epidermis of the recipient. Thus, for example, the active ingredientcan be delivered from the plaster by iontophoresis, as described ingeneral terms in Pharmaceutical Research, 3(6), 318 (1986).

Pharmaceutical compounds adapted for topical administration can beformulated as ointments, creams, suspensions, lotions, powders,solutions, pastes, gels, sprays, aerosols or oils.

For the treatment of the eye or other external tissue, for example mouthand skin, the formulations are preferably applied as topical ointment orcream. In the case of formulation to give an ointment, the activeingredient can be employed either with a paraffinic or a water-misciblecream base. Alternatively, the active ingredient can be formulated togive a cream with an oil-in-water cream base or a water-in-oil base.

Pharmaceutical formulations adapted for topical application to the eyeinclude eye drops, in which the active ingredient is dissolved orsuspended in a suitable carrier, in particular an aqueous solvent.

Pharmaceutical formulations adapted for topical application in the mouthencompass lozenges, pastilles and mouthwashes.

Pharmaceutical formulations adapted for rectal administration can beadministered in the form of suppositories or enemas.

Pharmaceutical formulations adapted for nasal administration in whichthe carrier substance is a solid comprise a coarse powder having aparticle size, for example, in the range 20-500 microns, which isadministered in the manner in which snuff is taken, i.e. by rapidinhalation via the nasal pas-sages from a container containing thepowder held close to the nose. Suitable formulations for administrationas nasal spray or nose drops with a liquid as carrier substanceencompass active-ingredient solutions in water or oil.

Pharmaceutical formulations adapted for administration by inhalationencompass finely particulate dusts or mists, which can be generated byvarious types of pressurised dispensers with aerosols, nebulisers orinsufflators.

Pharmaceutical formulations adapted for vaginal administration can beadministered as pessaries, tampons, creams, gels, pastes, foams or sprayformulations.

Pharmaceutical formulations adapted for parenteral administrationinclude aqueous and non-aqueous sterile injection solutions comprisingantioxidants, buffers, bacteriostatics and solutes, by means of whichthe formulation is rendered isotonic with the blood of the recipient tobe treated; and aqueous and non-aqueous sterile suspensions, which maycomprise suspension media and thickeners. The formulations can beadministered in single-dose or multidose containers, for example sealedampoules and vials, and stored in freeze-dried (lyophilised) state, sothat only the addition of the sterile carrier liquid, for example waterfor injection purposes, immediately before use is necessary. Injectionsolutions and suspensions prepared in accordance with the recipe can beprepared from sterile powders, granules and tablets.

It goes without saying that, in addition to the above particularlymentioned constituents, the formulations may also comprise other agentsusual in the art with respect to the particular type of formulation;thus, for example, formulations which are suitable for oraladministration may comprise flavours.

A therapeutically effective amount of a compound of the formula Idepends on a number of factors, including, for example, the age andweight of the animal, the precise condition that requires treatment, andits severity, the nature of the formulation and the method ofadministration, and is ultimately determined by the treating doctor orvet. However, an effective amount of a compound according to theinvention is generally in the range from 0.1 to 100 mg/kg of body weightof the recipient (mammal) per day and particularly typically in therange from 1 to 10 mg/kg of body weight per day. Thus, the actual amountper day for an adult mammal weighing 70 kg is usually between 70 and 700mg, where this amount can be administered as a single dose per day orusually in a series of part-doses (such as, for example, two, three,four, five or six) per day, so that the total daily dose is the same. Aneffective amount of a salt or solvate or of a physiologically functionalderivative thereof can be determined as the fraction of the effectiveamount of the compound according to the invention per se. It can beassumed that similar doses are suitable for the treatment of otherconditions mentioned above.

A combined treatment of this type can be achieved with the aid ofsimultaneous, consecutive or separate dispensing of the individualcomponents of the treatment. Combination products of this type employthe compounds according to the invention.

The invention furthermore relates to medicaments comprising at least onecompound of the formula I and/or pharmaceutically acceptable salts,tautomers and stereoisomers thereof, including mixtures thereof in allratios, and at least one further medicament active ingredient.

The invention also relates to a set (kit) consisting of separate packsof

-   (a) an effective amount of a compound of the formula I and/or    pharmaceutically acceptable salts, tautomers and stereoisomers    thereof, including mixtures thereof in all ratios, and-   (b) an effective amount of a further medicament active ingredient.

The set comprises suitable containers, such as boxes, individualbottles, bags or ampoules. The set may, for example, comprise separateampoules, each containing an effective amount of a compound of theformula I and/or pharmaceutically acceptable salts, tautomers andstereoisomers thereof, including mixtures thereof in all ratios,

and an effective amount of a further medicament active ingredient indissolved or lyophilised form.

“Treating” as used herein, means an alleviation, in whole or in part, ofsymptoms associated with a disorder or disease, or slowing, or haltingof further progression or worsening of those symptoms, or prevention orprophylaxis of the disease or disorder in a subject at risk fordeveloping the disease or disorder.

The term “effective amount” in connection with a compound of formula Ican mean an amount capable of alleviating, in whole or in part, symptomsassociated with a disorder or disease, or slowing or halting furtherprogression or worsening of those symptoms, or preventing or providingprophylaxis for the disease or disorder in a subject having or at riskfor developing a disease disclosed herein, such as inflammatoryconditions, immunological conditions, cancer or metabolic conditions.

In one embodiment an effective amount of a compound of formula I is anamount that inhibits c-KIT kinase in a cell, such as, for example, invitro or in vivo. In some embodiments, the effective amount of thecompound of formula I inhibits tankyrase in a cell by 10%, 20%, 30%,40%, 50%, 60%, 70%, 80%, 90% or 99%, compared to the activity of c-KITkinase in an untreated cell. The effective amount of the compound offormula I, for example in a pharmaceutical composition, may be at alevel that will exercise the desired effect; for example, about 0.005mg/kg of a subject's body weight to about 10 mg/kg of a subject's bodyweight in unit dosage for both oral and parenteral administration.

Use

The present compounds are suitable as pharmaceutical active ingredientsfor mammals, especially for humans, in the treatment of cancer, such asgastrointestinal stromal tumor.

The present invention encompasses the use of the compounds of theformula I and/or pharmaceutically acceptable salts, tautomers andstereoisomers thereof for the preparation of a medicament for thetreatment or prevention of cancer, preferably for the treatment ofgastrointestinal stromal tumor.

Preferably, the present invention relates to a method for treating adisease, wherein the disease is a cancer, preferably a gastrointestinalstromal tumor.

Particularly preferable, the present invention relates to a methodwherein the disease is a cancer, wherein administration is simultaneous,sequential or in alternation with administration of at least one otheractive drug agent.

The disclosed compounds of the formula I can be administered incombination with other known therapeutic agents, including anticanceragents. As used here, the term “anticancer agent” relates to any agentwhich is administered to a patient with cancer for the purposes oftreating the cancer.

The anti-cancer treatment defined above may be applied as a monotherapyor may involve, in addition to the herein disclosed compounds of formulaI, conventional surgery or radiotherapy or medicinal therapy. Suchmedicinal therapy, e.g. a chemotherapy or a targeted therapy, mayinclude one or more, but preferably one, of the following anti-tumoragents:

Alkylating Agents

such as altretamine, bendamustine, busulfan, carmustine, chlorambucil,chlormethine, cyclophosphamide, dacarbazine, ifosfamide, improsulfan,tosilate, lomustine, melphalan, mitobronitol, mitolactol, nimustine,ranimustine, temozolomide, thiotepa, treosulfan, mechloretamine,carboquone; apaziquone, fotemustine, glufosfamide, palifosfamide,pipobroman, trofosfamide, uramustine, TH-302⁴, VAL-083⁴;

Platinum Compounds

such as carboplatin, cisplatin, eptaplatin, miriplatine hydrate,oxaliplatin, lobaplatin, nedaplatin, picoplatin, satraplatin;lobaplatin, nedaplatin, picoplatin, satraplatin;

DNA Altering Agents

such as amrubicin, bisantrene, decitabine, mitoxantrone, procarbazine,trabectedin, clofarabine;

amsacrine, brostallicin, pixantrone, laromustine^(1,3);

Topoisomerase Inhibitors

such as etoposide, irinotecan, razoxane, sobuzoxane, teniposide,topotecan; amonafide, belotecan, elliptinium acetate, voreloxin;

Microtubule Modifiers

such as cabazitaxel, docetaxel, eribulin, ixabepilone, paclitaxel,vinblastine, vincristine, vinorelbine, vindesine, vinflunine;

fosbretabulin, tesetaxel;

Antimetabolites

such as asparaginase³, azacitidine, calcium levofolinate, capecitabine,cladribine, cytarabine, enocitabine, floxuridine, fludarabine,fluorouracil, gemcitabine, mercaptopurine, methotrexate, nelarabine,pemetrexed, pralatrexate, azathioprine, thioguanine, carmofur;

doxifluridine, elacytarabine, raltitrexed, sapacitabine, tegafur^(2,3),trimetrexate;

Anticancer Antibiotics

such as bleomycin, dactinomycin, doxorubicin, epirubicin, idarubicin,levamisole, miltefosine, mitomycin C, romidepsin, streptozocin,valrubicin, zinostatin, zorubicin, daunurobicin, plicamycin;

aclarubicin, peplomycin, pirarubicin;

Hormones/Antagonists

such as abarelix, abiraterone, bicalutamide, buserelin, calusterone,chlorotrianisene, degarelix, dexamethasone, estradiol, fluocortolonefluoxymesterone, flutamide, fulvestrant, goserelin, histrelin,leuprorelin, megestrol, mitotane, nafarelin, nandrolone, nilutamide,octreotide, prednisolone, raloxifene, tamoxifen, thyrotropin alfa,toremifene, trilostane, triptorelin, diethylstilbestrol;

acolbifene, danazol, deslorelin, epitiostanol, orteronel,enzalutamide^(1,3);

Aromatase Inhibitors

such as aminoglutethimide, anastrozole, exemestane, fadrozole,letrozole, testolactone;

formestane;

Small Molecule Kinase Inhibitors

such as crizotinib, dasatinib, erlotinib, imatinib, lapatinib,nilotinib, pazopanib, regorafenib, ruxolitinib, sorafenib, sunitinib,vandetanib, vemurafenib, bosutinib, gefitinib, axitinib;

afatinib, alisertib, dabrafenib, dacomitinib, dinaciclib, dovitinib,enzastaurin, nintedanib, lenvatinib, linifanib, linsitinib, masitinib,midostaurin, motesanib, neratinib, orantinib, perifosine, ponatinib,radotinib, rigosertib, tipifarnib, tivantinib, tivozanib, trametinib,pimasertib, brivanib alaninate, cediranib, apatinib⁴, cabozantinibS-malate^(1,3), ibrutinib^(1,3), icotinib⁴, buparlisib², cipatinib⁴,cobimetinib^(1,3), idelalisib^(1,3), fedratinib¹, XL-647⁴;

Photosensitizers

such as methoxsalen³;

porfimer sodium, talaporfin, temoporfin;

Antibodies

such as alemtuzumab, besilesomab, brentuximab vedotin, cetuximab,denosumab, ipilimumab, ofatumumab, panitumumab, rituximab, tositumomab,trastuzumab, bevacizumab, pertuzumab^(2,3;)

catumaxomab, elotuzumab, epratuzumab, farletuzumab, mogamulizumab,necitumumab, nimotuzumab, obinutuzumab, ocaratuzumab, oregovomab,ramucirumab, rilotumumab, siltuximab, tocilizumab, zalutumumab,zanolimumab, matuzumab, dalotuzumab^(1,2,3), onartuzumab^(1,3),racotumomab¹, tabalumab^(1,3), EMD-525797⁴, nivolumab^(1,3);

Cytokines

such as aldesleukin, interferon alfa², interferon alfa2a³, interferonalfa2b^(2,3); celmoleukin, tasonermin, teceleukin, oprelvekin^(1,3),recombinant interferon beta-1a⁴;

Drug Conjugates

such as denileukin diftitox, ibritumomab tiuxetan, iobenguane 1123,prednimustine, trastuzumab emtansine, estramustine, gemtuzumab,ozogamicin, aflibercept;

cintredekin besudotox, edotreotide, inotuzumab ozogamicin, naptumomabestafenatox, oportuzumab monatox, technetium (99mTc) arcitumomab^(1,3),vintafolid^(1,3);

Vaccines

such as sipuleucel³; vitespen³, emepepimut-S³, oncoVAX⁴, rindopepimut³,troVax⁴, MGN-1601⁴, MGN-1703⁴;

Miscellaneous

alitretinoin, bexarotene, bortezomib, everolimus, ibandronic acid,imiquimod, lenalidomide, lentinan, metirosine, mifamurtide, pamidronicacid, pegaspargase, pentostatin, sipuleucel³, sizofiran, tamibarotene,temsirolimus, thalidomide, tretinoin, vismodegib, zoledronic acid,vorinostat;

celecoxib, cilengitide, entinostat, etanidazole, ganetespib, idronoxil,iniparib, ixazomib, lonidamine, nimorazole, panobinostat, peretinoin,plitidepsin, pomalidomide, procodazol, ridaforolimus, tasquinimod,telotristat, thymalfasin, tirapazamine, tosedostat, trabedersen,ubenimex, valspodar, gendicine⁴, picibanil⁴, reolysin⁴, retaspimycinhydrochloride^(1,3), trebananib^(2,3), virulizin⁴, carfilzomib^(1,3,)endostatin⁴, immucothel⁴, belinostat³, MGN-1703⁴;

¹ Prop. INN (Proposed International Nonproprietary Name)

² Rec. INN (Recommended International Nonproprietary Names)

³ USAN (United States Adopted Name)

⁴ no INN.

The following abbreviations refer respectively to the definitions below:

aq (aqueous), h (hour), g (gram), L (liter), mg (milligram), MHz(Megahertz), min. (minute), mm (millimeter), mmol (millimole), mM(millimolar), m.p. (melting point), eq (equivalent), mL (milliliter), L(microliter), ACN (acetonitrile), AcOH (acetic acid), CDCl₃ (deuteratedchloroform), CD₃OD (deuterated methanol), CH₃CN (acetonitrile), c-hex(cyclohexane), DCC (dicyclohexyl carbodiimide), DCM (dichloromethane),DIC (diisopropyl carbodiimide), DIEA (diisopropylethyl-amine), DMF(dimethylformamide), DMSO (dimethylsulfoxide), DMSO-d₆ (deuterateddimethylsulfoxide), EDC(1-(3-dimethyl-amino-propyl)-3-ethylcarbodiimide), ESI (Electro-sprayionization), EtOAc (ethyl acetate), Et₂O (diethyl ether), EtOH(ethanol), HATU(dimethylamino-([1,2,3]triazolo[4,5-b]pyridin-3-yloxy)-methylene]-dimethyl-ammoniumhexafluorophosphate), HPLC (High Performance Liquid Chromatography),i-PrOH (2-propanol), K₂CO₃ (potassium carbonate), LC (LiquidChromatography), MeOH (methanol), MgSO₄ (magnesium sulfate), MS (massspectrometry), MTBE (Methyl tert-butyl ether), NaHCO₃(sodiumbicarbonate), NaBH₄ (sodium borohydride), NMM (N-methyl morpholine), NMR(Nuclear Magnetic Resonance), PyBOP(benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphoniumhexafluorophosphate), RT (room temperature), Rt (retention time), SPE(solid phase extraction), TBTU(2-(1-H-benzotriazole-1-yl)-1,1,3,3-tetramethyluromium tetrafluoroborate), TEA (triethylamine), TFA (trifluoroacetic acid), THF(tetrahydrofuran), TLC (Thin Layer Chromatography), UV (Ultraviolet).

Above and below, all temperatures are indicated in ° C. In the followingexamples, “conventional work-up” means: water is added if necessary, thepH is adjusted, if necessary, to values between 2 and 10, depending onthe constitution of the end product, the mixture is extracted with ethylacetate or dichloromethane, the phases are separated, the organic phaseis dried over sodium sulfate and evaporated, and the residue is purifiedby chromatography on silica gel and/or by crystallisation. Rf values onsilica gel; eluent: ethyl acetate/methanol 9:1.

¹H NMR was recorded on Bruker DPX-300, DRX-400, AVII-400 or on a 500 MHzspectrometer, using residual signal of deuterated solvent as internalreference. Chemical shifts (6) are reported in ppm relative to theresidual solvent signal (δ=2.49 ppm for ¹H NMR in DMSO-d₆). ¹H NMR dataare reported as follows: chemical shift (multiplicity, couplingconstants, and number of hydrogens). Multiplicity is abbreviated asfollows: s (singlet), d (doublet), t (triplet), q (quartet), m(multiplet), br (broad).

HPLC/MS conditions A:

HPLC/MS: Agilent 1200/6100

eluent A: water+0.05% formic acid

eluent B: acetonitrile+0.04% formic acid

column: Chromolith HR RP-18e; 50-4.6 mm

flow rate: 3.3 ml/min

gradient: 0%->100% B: 0.0->2.0 min|100% B: 2.0->2.5 min

UV detection: 220 nm

MS detection: 65-800 amu positive

HPLC/MS conditions B:

HPLC/MS: Agilent 1200/6100

eluent A: water+0.05% formic acid

eluent B: acetonitrile+0.04% formic acid

column: Kinetex XB-C18; 2.6 μm; 50-4.6 mm

flow rate: 2.5 ml/min

gradient: 0%->100% B: 0.0->1.4 min|100% B: 1.4->2.0 min

UV detection: 220 nm

MS detection: 65-800 amu positive

UPLC/MS conditions:

UPLC/MS: Waters Acquity/SQD

eluent A: water+0.05% formic acid

eluent B: acetonitrile+0.04% formic acid

column: Kinetex XB-C18; 1.7 μm; 50-2.1 mm

flow rate: 0.9 ml/min

gradient: 2%->100% B: 0.0->1.0 min|100% B: 1.0->1.3 min

UV detection: 220 nm/254 nm/MaxPlot/TotalPlot

MS detection: 61-800 amu positive

Assays

c-Kit(V654A) assay:

c-Kit(V654A) (N-terminal GST-tagged, recombinant human c-Kit, aminoacids 544-end containing the V654A mutation) is incubated with 8 mM MOPSpH 7.0, 0.2 mM EDTA, 250 μM GGMEDIYEFMGGKKK, 10 mM MgAcetate and[gamma-33P-ATP] (specific activity approx. 500 cpm/pmol, concentration200 μM). The reaction is initiated by the addition of the MgATP mix.After incubation for 40 minutes at room temperature, the reaction isstopped by the addition of 3% phosphoric acid solution. 10 μL of thereaction is then spotted onto a P30 filtermat and washed three times for5 minutes in 75 mM phosphoric acid and once in methanol prior to dryingand scintillation counting.

PDGFRalpha(V561 D) assay:

PDGFRalpha(V561 D) (N-terminal 6His-tagged, recombinant humanPDGFRalpha, amino acids 550-end containing the V561 D mutation) isincubated with 8 mM MOPS pH 7.0, 0.2 mM EDTA, 250 μM GGMEDIYEFMGGKKK, 10mM MgAcetate and [gamma-33P-ATP] (specific activity approx. 500cpm/pmol, concentration 200 μM). The reaction is initiated by theaddition of the MgATP mix. After incubation for 40 minutes at roomtemperature, the reaction is stopped by the addition of 3% phosphoricacid solution. 10 μL of the reaction is then spotted onto a P30filtermat and washed three times for 5 minutes in 75 mM phosphoric acidand once in methanol prior to drying and scintillation counting.

Pharmacological Data

TABLE 1 Inhibition (IC₅₀) of c-KIT (V654A) and PDGFRα (V561D) ofcompounds of the formula I Compound c-KIT PDGFRα Compound c-KIT PDGFRαNo. (V654A) [M] (V561D) [M] No. (V654A) [M] (V561D) [M] “A1”  6E−09 2E−09 “A81” 1.7E−08  6E−09 “A2” 5.1E−08 1.2E−08 “A82” 1.4E−08  3E−09“A3” 5.3E−08 1.6E−08 “A83”  1E−08  3E−09 “A4” 3.4E−08 1.9E−08 “A84”4.8E−08  5E−09 “A5” “A85” 1.3E−06 1.7E−06 “A6” 4.3E−07 “A86” 1.1E−08 2E−09 “A7” 4.9E−07 “A87” 2.5E−08 1.2E−08 “A8” 1.7E−07 1.4E−08 “A88” 9E−08  6E−09 “A9” 7.6E−07 2.3E−07 “A89” 3.6E−08  8E−09 “A10” 8.2E−083.2E−08 “A90”  2E−08 2.9E−08 “A11” 2.2E−07 2.6E−08 “A91” 1.9E−08 8.2E−09“A12” 6.9E−08 6.3E−08 “A92” 2.1E−08 5.9E−09 “A13”  5E−07 “A93” 3.2E−073.1E−07 “A14” 2.3E−08  2E−08 “A94” 3.6E−06 2.3E−06 “A94a” 6.0E−085.4E−08 “A15” 4.9E−08 4.7E−08 “A95” 9.0E−09 3.7E−07 “A16” 3.3E−08 “A96”5.2E−09 3.3E−10 “A17” 2.9E−07 6.7E−08 “A97” 1.7E−08 1.0E−08 “A18”1.5E−08  5E−09 “A98” 1.8E−07 7.5E−08 “A19” 3.8E−08 1.4E−08 “A99” 3.3E−087.6E−08 “A20”  2E−07 5.2E−08 “A100”  2E−08 6.3E−08 “A100a” 1.8E−085.4E−08 “A21” 7.9E−08 3.2E−08 “A101” 3.3E−08 2.9E−07 “A22” 2.7E−08 6E−09 “A102” 1.1E−08 4.8E−08 “A23” 2.5E−07 “A103” 8.6E−09 3.5E−08 “A24”1.1E−07 2.6E−08 “A104” 2.4E−08 1.5E−07 “A25” 1.5E−08  3E−09 “A105”9.7E−09 3.4E−07 “A26” 1.5E−08  1E−08 “A106” 9.1E−09  9E−10 “A27”  5E−083.2E−08 “A107” 4.4E−08 2.3E−08 “A28” 3.6E−08 2.9E−08 “A108” 8.3E−088.1E−08 “A29” 1.5E−07 2.3E−08 “A109” 1.2E−08 3.4E−09 “A30” 2.2E−061.5E−07 “A110” 3.9E−08 2.8E−08 “A31” 9.9E−08 1.3E−08 “A111” 7.7E−091.8E−08 “A32” 6.4E−08 1.1E−08 “A112” 1.6E−08 6.4E−08 “A33”  2E−08  3E−09“A113” 8.6E−09 3.6E−08 “A34” 5.8E−06 1.1E−07 “A114” 2.0E−08 1.4E−07“A35” 6.5E−07 4.9E−08 “A115” 1.8E−07 1.4E−06 “A115a” 1.6E−07 1.5E−06“A36” 2.9E−08 1.7E−08 “A116” “A37” 3.8E−08  9E−09 “A117” 2.8E−08 1.1E−08“A38” 3.2E−06 5.8E−7  “A118” 1.6E−08  5E−09 “A39” 7.4E−08 2.3E−08 “A119” 9E−09 4.6E−08 “A40” 2.6E−08  7E−09 “A120” 2.8E−07 2.3E−07 “A41” 2.4E−074.4E−08 “A121”  4E−08 1.6E−08 “A42” 8.4E−08 3.8E−08 “A122” 7.3E−08 5E−09 “A43” 1.4E−07 1.7E−07 “A123”  5E−09  1E−09 “A44” “A124” 6.6E−08 9E−09 “A45” 1.1E−06 3.3E−07 “A125” 3.4E−08  6E−09 “A46” 3.7E−07 1.5E−07“A126” 1.9E−08 4.2E−08 “A47” 2.4E−08  7E−09 “A127” 3.8E−08 7.9E−08 “A48”1.7E−08 1.9E−08 “A128” 4.1E−08 9.7E−09 “A49” 1.5E−07 4.2E−08 “A129”1.3E−08 4.8E−08 “A50” 2.4E−08 1.4E−08 “A130” 3.5E−08 1.7E−07 “A51”9.1E−08 2.2E−08 “A131” 9.7E−09 3.8E−08 “A52” 2.2E−08 2.7E−08 “A132”7.5E−09  8E−10 “A53” 1.1E−08  9E−09 “A133” 1.1E−08 6.4E−09 “A54” 4.9E−071.6E−07 “A134” 1.7E−08 1.6E−08 “A55” 1.4E−08 1.4E−08 “A135” 1.8E−073.1E−07 “A56”  7E−09  5E−09 “A136” 1.5E−08 1.8E−08 “A57” 1.5E−08  6E−09“A137” 4.0E−08 4.2E−08 “A58” 4.4E−08 2.1E−08 “A138” 1.1E−08 8.6E−08“A59” 7.6E−08 4.6E−08 “A139” 1.2E−08 3.8E−06 “A60” 3.8E−08 3.3E−08“A140” 1.4E−08 2.8E−08 “A61” 2.9E−08 1.1E−08 “A141” 3.8E−09 2.8E−09“A62”  2E−07 4.6E−08 “A142” 2.8E−07 2.8E−06 “A63” 1.3E−07  4E−08 “A143”1.9E−08 3.1E−07 “A64” 4.4E−08 1.6E−08 “A144” 1.2E−08 1.7E−07 “A65”1.2E−06 1.5E−07 “A145” 2.2E−08 1.8E−07 “A66” 6.4E−07 1.9E−07 “A146”“A67” 2.4E−08  4E−09 “A147” “A68” 2.8E−08  7E−09 “A148” “A69” 1.4E−08 1E−08 “A149”  6E−09 1.2E−08 “A70” 1.4E−08  5E−09 “A150” 4.9E−08 3.7E−08“A71”  8E−09  4E−09 “A151”  3E−09  1E−09 “A72” 1.1E−08  4E−09 “A152”1.1E−08 2.3E−08 “A73” 4.4E−07 “A153” 2.4E−08  4E−09 “A74”  8E−09  6E−09“A154” 1.1E−08  3E−09 “A75” 4.8E−08 1.8E−08 “A155” 8.1E−08 6.1E−08 “A76”4.9E−08  3E−08 “A156” 2.6E−08 4.0E−08 “A77” 4.7E−07 1.1E−07 “A157”5.9E−09 3.2E−10 “A78” 1.7E−08 3.1E−08 “A158” 1.3E−08 4.6E−08 “A79”3.3E−08 3.1E−08 “A159”  2E−08 9.1E−08 “A80” 1.2E−07 4.4E−08 “A160”1.6E−08 7.5E−08 “A161” 3.5E−08 1.5E−08 “A171” 1.7E−08 1.9E−07 “A162”8.2E−08 9.7E−08 “A172” 6.3E−09 2.5E−08 “A163” 9.9E−09 4.5E−08 “A173”“A164” 8.4E−09 1.1E−08 “A174” “A165” 3.0E−08 3.3E−08 “A175” 9.2E−08 6E−09 “A166” 8.0E−09 4.3E−08 “A176” 6.7E−09 1.6E−09 “A167” 1.8E−082.1E−08 “A177” 1.7E−07 5.7E−08 “A168” 3.7E−08 1.0E−07 “A178” 3.9E−091.3E−09 “A169” 1.4E−08 4.3E−07 “A179” 1.4E−08 1.6E−09 “A170” 1.8E−061.2E−05 “A180” 9.5E−09 5.0E−10 “A181” 8.5E−09 7.1E−10 “A191” 1.5E−082.4E−07 “A182” 1.3E−08 1.2E−09 “A192” 2.3E−07 2.0E−07 “A183” 7.5E−092.6E−08 “A193” 2.3E−07 2.0E−07 “A184” 1.8E−08 1.1E−08 “A194” 4.9E−089.1E−08 “A185” 5.1E−07 “A195” 6.8E−08 9.3E−08 “A186” “A196” 4.4E−081.1E−07 “A187” 3.6E−08 7.6E−08 “A197” 2.8E−08 3.2E−08 “A188” 2.6E−081.6E−06 “A198” 3.0E−08 2.0E−07 “A189” 1.1E−07 4.3E−07 “A199” 1.6E−082.2E−08 “A190” 9.7E−09 6.4E−08 “A200” 1.8E−07 1.4E−07 “A201” 9.7E−089.2E−08 “A211” 1.9E−07 8.5E−08 “A202” 5.7E−08 1.6E−08 “A212” 1.3E−061.6E−07 “A203” 3.6E−08 4.9E−07 “A213” 6.5E−08 3.7E−08 “A204” 5.5E−081.1E−07 “A214” 7.2E−08 7.9E−08 “A205” 3.6E−08 9.4E−08 “A215” 6.4E−082.2E−07 “A206” 2.4E−08 4.8E−08 “A216” 5.2E−08 2.9E−08 “A207” 5.2E−083.1E−07 “A217” 3.5E−07 4.6E−08 “A208” 1.8E−08 1.8E−07 “A218” 6.4E−085.9E−08 “A209” 5.3E−08 5.8E−07 “A219” 1.6E−06 3.2E−07 “A210” 4.6E−083.0E−07 “A220” 9.8E−07 5.0E−07 “A221” 2.0E−07 3.8E−07 “A231” 9.0E−083.4E−07 “A222” 7.2E−08 2.1E−07 “A232” 1.6E−07 9.8E−07 “A223” 3.5E−074.1E−07 “A233” 9.6E−08 6.0E−07 “A224” 7.0E−08 2.8E−07 “A234” 5.0E−087.4E−07 “A225” 1.9E−07 5.8E−07 “A235” 4.2E−08 1.4E−07 “A226” 5.5E−088.9E−08 “A236” 5.3E−08 5.6E−07 “A227” 9.2E−08 1.4E−07 “A237” 8.1E−084.9E−07 “A228” 7.4E−08 3.0E−07 “A238” 7.9E−08 6.2E−07 “A229” 4.1E−081.5E−07 “A239” 3.3E−07 1.2E−06 “A230” 4.9E−08 9.5E−08 “A240” 1.3E−072.5E−07 “A241” 1.0E−07 2.9E−07 “A251” 1.6E−07 4.0E−07 “A242” 1.1E−081.7E−08 “A252” 9.8E−08 9.3E−08 “A243” 3.0E−08 1.4E−08 “A253” 4.4E−082.1E−08 “A244” 3.6E−08 1.3E−08 “A254” 5.7E−08 2.4E−08 “A245” 6.5E−084.7E−07 “A255” 2.2E−08 2.6E−09 “A246” 2.3E−08 7.4E−09 “A256” 2.7E−084.3E−09 “A247” 2.3E−08 4.5E−08 “A257” 2.7E−08 3.7E−09 “A248” 3.5E−084.5E−08 “A258” 4.7E−08 8.6E−08 “A249” 3.5E−08 2.6E−07 “A259” 5.7E−088.4E−09 “A250”  4E−08 7.6E−08 “A260” 5.1E−08 1.0E−07 “A261” 4.4E−083.7E−08 “A271”  5E−08 5.1E−10 “A262” 9.4E−08 1.1E−07 “A272” 4.8E−088.9E−10 “A263” 9.4E−08 9.1E−10 “A273”  4E−08 4.1E−09 “A264” 7.5E−081.2E−09 “A274” 6.1E−08 3.3E−09 “A265” 4.9E−08 1.6E−09 “A275” 4.5E−082.1E−10 “A266” 4.0E−08 1.1E−09 “A276” 5.4E−08 1.4E−09 “A267” 1.7E−081.4E−09 “A277”  3E−08 2.6E−09 “A268” 1.6E−08 6.7E−10 “A278” 1.7E−081.5E−09 “A269” 3.1E−08 1.5E−09 “A279” 1.4E−08 7.2E−10 “A270” 2.6E−08 2E−10 “A280” 7.7E−08 5.3E−08 “A281” 5.7E−08 1.0E−08 “A291” 7.5E−09“A282” 1.6E−08 “A292” “A283” 1.9E−08 “A293” “A284” 1.7E−08 “A294” “A285”5.6E−09 “A295” “A286” 5.1E−09 “A296” 3.8E−08 1.4E−08 “A287” 2.5E−08“A297” 6.6E−08 2.4E−07 “A288” 6.5E−09 “A298” 4.1E−08 2.1E−08 “A289”2.5E−08 “A299” 5.8E−08 2.3E−08 “A290” 1.4E−08 “A300” 6.8E−08 7.6E−10“A301” 4.3E−08 1.0E−09 “A311” 2.1E−08 3.1E−07 “A302” 3.1E−08 1.2E−09“A312” 6.1E−08 2.9E−07 “A303” 3.7E−08  6E−09 “A313” 2.6E−08 3.3E−07“A304” 1.6E−08 “A314” 7.2E−08 1.8E−07 “A305” 7.7E−09 “A315” 2.0E−071.4E−06 “A306” 4.5E−08 2.4E−07 “A316” 1.2E−07 5.2E−07 “A307” 1.7E−082.4E−07 “A317” 1.2E−07 1.4E−06 “A308” 1.0E−08 9.74E−08  “A318”  2E−081.7E−08 “A309” 6.3E−08 1.3E−07 “A319” 2.7E−08 3.6E−08 “A310” 4.4E−088.5E−08 “A320” 4.8E−08 9.9E−08 “A321” 4.4E−08 3.7E−07 “A331” 6.3E−085.7E−07 “A322” 2.5E−08 6.5E−08 “A332” 7.1E−08 1.0E−07 “A323” 2.2E−072.2E−07 “A333” 6.3E−08 1.2E−07 “A324” 2.7E−07 7.2E−09 “A334” 1.5E−084.1E−08 “A325” 1.7E−08 3.8E−09 “A335” 1.7E−07 6.8E−07 “A326” 1.8E−079.4E−07 “A336” 1.8E−07 2.4E−07 “A327” 1.4E−08 2.2E−07 “A337” 7.5E−082.3E−07 “A328” 4.0E−08 9.7E−08 “A338” 3.9E−08 1.6E−07 “A329” 7.3E−089.2E−08 “A339” 9.2E−09 “A330” 4.8E−08 2.1E−08 “A340” “A341” “A351”1.4E−08 “A342” 2.5E−08 3.6E−08 “A352” 2.6E−07 4.4E−07 “A343”  9E−098.5E−08 “A353” 9.4E−08 1.9E−07 “A344” 9.7E−09 1.6E−08 “A354” 3.1E−064.2E−07 “A345” 1.2E−08 1.5E−06 “A355” 8.9E−08 1.6E−06 “A346” 1.6E−08“A356” 9.6E−08 1.5E−07 “A347” 2.6E−08 “A357” “A348” 1.6E−08 “A358”1.9E−08 “A349” 5.1E−08 “A359” 1.3E−08 “A350” 1.6E−08 “A360” 2.2E−08“A361” 1.1E−08 “A371” 3.4E−08 1.1E−08 “A362” 1.6E−08 “A372” 2.1E−08“A363” “A373” 1.5E−08 “A364” 2.1E−08 “A374” 1.7E−08 “A365” “A375”9.5E−09 “A366” “A376” 4.9E−09 “A367” 1.9E−08 7.0E−08 “A368” 2.3E−083.4E−08 “A369” 1.3E−08 3.4E−08 “A370” 3.1E−08 5.8E−08

Explanation: 1.4E-06 means 1.4×10⁻⁶

The compounds shown in Table 1 are particularly preferred compoundsaccording to the invention.

Synthesis of Intermediates Bromoquinolones and bromonaphthyridonesSynthesis of 3-bromo-6-fluoro-1H-quinolin-2-one

A solution of 2-amino-5-fluoro-benzaldehyde (7.42 g, 53.3 mmol) indimethyl malonate (45 ml) is heated to 140° C. and stirred at thistemperature for 16 hours. The reaction mixture is allowed to reach roomtemperature. The resultant precipitate is filtered off, washed withtert-butyl methyl ether and dried under vacuum to afford6-fluoro-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid methyl ester aslight ochre solid; HPLC/MS 1.17 min (B), [M+H]⁺ 222.

¹H NMR (400 MHz, DMSO-d₆) δ 12.11 (s, 1H), 8.49 (s, 1H), 7.70 (dd,J=9.0, 2.9 Hz, 1H), 7.52 (td, J=8.9, 2.9 Hz, 1H), 7.35 (dd, J=9.1, 4.7Hz, 1H), 3.81 (s, 3H).

To a slurry of 6-fluoro-2-oxo-1,2-dihydro-quinoline-3-carboxylic acidmethyl ester (6.92 g, 31.3 mmol) in a mixture of THF (30 ml) and water(38 ml) is added lithium hydroxide (6.59 g, 275 mmol) and the mixture isstirred for 2 hours at 65° C. After cooling to room temperature, 1 Naqueous hydrochloric acid is added until a pH value of 1 is reached. Theresultant precipitate is filtered off, washed with water and dried undervacuum to afford 6-fluoro-2-oxo-1,2-dihydro-quinoline-3-carboxylic acidas light yellow solid; HPLC/MS 1.18 min (B), [M+H]+ 208.

A suspension of 6-fluoro-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid(6.70 g, 32.3 mmol) in pyridine (108 ml) is cooled to 0° C. Understirring and continuous external cooling, bromine (6.63 ml, 129 mmol) isadded dropwise. The reaction mixture is heated to 65° C. and stirred atthis temperature for 1 hour. After cooling to room temperature, thereaction mixture is poured into water (160 ml). 37% aqueous hydrochloricacid is added until a pH value of 4 is reached. The resultantprecipitate is filtered off and washed with water. The filtrate isextracted three times with dichloromethane; the organic phases arecombined, dried over sodium sulfate and evaporated. The residue iscombined with the precipitate and chromatographed on a silica gel columnwith dichloromethane/methanol as eluent to afford3-bromo-6-fluoro-1H-quinolin-2-one as light yellow solid; HPLC/MS 1.26min (B), [M+H]⁺ 242,244.

¹H NMR (400 MHz, DMSO-d₆) δ 12.31 (s, 1H), 8.49 (s, 1H), 7.54 (dd,J=9.1, 2.8 Hz, 1H), 7.46 (td, J=8.8, 2.8 Hz, 1H), 7.36 (dd, J=9.0, 4.8Hz, 1H).

The following compounds are prepared similarly

3-Bromo-6-chloro-1H-[1,8]naphthyridin-2-one, light brown solid; HPLC/MS1.24 min (B), [M+H]⁺ 261.

3-Bromo-6-methoxy-1H-[1,8]naphthyridin-2-one, brown solid; HPLC/MS 1.12min (B), [M+H]+ 255,257.

¹H NMR (400 MHz, DMSO-d6) δ 12.59 (s, 1H), 8.49 (s, 1H), 8.36 (d, J=3.0Hz, 1H), 7.75 (d, J=3.0 Hz, 1H), 3.86 (s, 3H).

3-Bromo-1H-[1,8]naphthyridin-2-one, brown solid; HPLC/MS 1.09 min (B),[M+H]⁺ 225,227.

¹H NMR (400 MHz, DMSO-d6) δ 12.74 (s, 1H), 8.56 (m, 2H), 8.13 (d, 1H),7.30 (dd, 1H).

3-Bromo-1H-[1,7]naphthyridin-2-one, orange-brown solid; HPLC/MS 1.00 min(B), [M+H]⁺ 225,227.

3-Bromo-7-methyl-1H-[1,8]naphthyridin-2-one, light yellow solid; HPLC/MS1.16 min (B), [M+H]⁺ 239,241.

3-Bromo-6-fluoro-1H-[1,8]naphthyridin-2-one, beige solid; HPLC/MS 1.15min (B), [M+H]+ 243,245.

¹H NMR (500 MHz, DMSO-d6) δ 12.80 (s, 1H), 8.62 (d, J=2.8 Hz, 1H), 8.52(s, 1H), 8.08 (dd, J=8.5, 2.9 Hz, 1H).

Ethynyl-Quinolones and Ethynyl-Naphthyridones Synthesis of3-ethynyl-1H-quinolin-2-one

To a suspension of 3-bromo-1H-quinolin-2-one (2.24 g, 10.0 mmol) indioxane (40 ml) are added triethylamine (3.67 ml, 26.5 mmol) andcopper(I) iodide (1.90 g, 10.0 mmol). The reaction mixture is purgedwith nitrogen and bis(triphenylphosphine)palladium(II) chloride (286 mg,0.40 mmol) and trimethylsilyl-acetylene (2.37 ml, 17.1 mmol) are added.The reaction mixture is flushed with nitrogen and stirred in a closedreaction vial for 16 hours at 80° C. The reaction mixture is allowed toreach room temperature and filtered through a plug of kieselguhr. Theresidue is washed with dichloromethane and the filtrate is evaporated.The residue is chromatographed on a silica gel column withcyclohexane/ethyl acetate as eluent to afford3-trimethylsilanylethynyl-1H-quinolin-2-one as light brown solid;HPLC/MS 1.52 min (B), [M+H]+ 242.

To a solution of 3-trimethylsilanylethynyl-1H-quinolin-2-one (2.16 g,8.95 mmol) in methanol (18 ml) is added potassium fluoride on aluminiumoxide (1.04 g, 5.7 mmol fluoride) and the reaction mixture is stirred atroom temperature for 30 minutes. The reaction mixture is poured into icewater. The solids are filtered off, washed with water and dried undervacuum. The residue is chromatographed on a silica gel column withdichloromethane/methanol as eluent to afford 3-ethynyl-1H-quinolin-2-oneas light brown solid; HPLC/MS 1.18 min (B), [M+H]+ 170.

1H NMR (400 MHz, DMSO-d₆) δ 12.02 (s, 1H), 8.23 (s, 1H), 7.67 (dd,J=7.9, 1.4 Hz, 1H), 7.53 (ddd, J=8.5, 7.2, 1.5 Hz, 1H), 7.34-7.27 (m,1H), 7.20 (ddd, J=8.1, 7.2, 1.1 Hz, 1H), 4.34 (s, 1H).

The following compounds are prepared similarly:

6-Chloro-3-ethynyl-1H-[1,8]naphthyridin-2-one, light beige solid;HPLC/MS 1.20 min (B), [M+H]⁺ 205.

3-Ethynyl-6-methoxy-1H-[1,8]naphthyridin-2-one, beige solid; HPLC/MS1.11 min (B), [M+H]⁺ 201.

¹H NMR (400 MHz, DMSO-d₆) δ 12.34 (s, 1H), 8.30 (d, J=3.0 Hz, 1H), 8.18(s, 1H), 7.72 (d, J=3.0 Hz, 1H), 4.41 (s, 1H), 3.84 (s, 3H).

3-Ethynyl-6-fluoro-1H-quinolin-2-one, beige solid; HPLC/MS 1.27 min (A),[M+H]⁺ 188.

3-Ethynyl-1H-[1,7]naphthyridin-2-one, beige powder; HPLC/MS 0.97 min(B), [M+H]⁺ 171;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (bs, 1H) 8.60 (s, 1H), 8.22 (d, J=5.2Hz, 1H), 8.14 (s, 1H), 7.51 (d, J=5.2 Hz, 1H), 4.41 (s, 1H).

3-Ethynyl-7-methyl-1H-[1,8]naphthyridin-2-one, beige solid; HPLC/MS 1.13min (B), [M+H]⁺ 185;

3-Ethynyl-6-fluoro-1H-[1,8]naphthyridin-2-one, orange-beige solid;HPLC/MS 1.11 min (B), [M+H]+ 189;

¹H NMR (500 MHz, DMSO-d₆) δ 12.45 (s, 1H), 8.47 (d, J=2.8 Hz, 1H), 8.10(s, 1H), 7.96 (dd, J=8.5, 3.0 Hz, 1H), 4.38 (s, 1H).

Aromatic Azides Synthesis of4-(4-azido-phenyl)-3-oxo-piperazine-1-carboxylic Acid Tert-Butyl Ester

To a stirred solution of4-(4-amino-phenyl)-3-oxo-piperazine-1-carboxylic acid tert-butyl ester(4.37 g, 15.0 mmol) in a mixture of ethanol (47 ml) and water (47 ml) isadded aqueous hydrochloric acid (37%, 9.15 ml). The solution is cooledto 0° C. and a solution sodium nitrite (1.24 g, 18.0 mmol) in water (10ml) is added slowly. The reaction mixture is stirred for 10 minutes atroom temperature. Then sodium azide (1.46 g, 22.5 mmol) is added inportions and the reaction mixture is stirred for 2 hours at roomtemperature. The reaction mixture is poured into water, the solids arefiltered off, washed with water and dried under vacuum to afford4-(4-azido-phenyl)-3-oxo-piperazine-1-carboxylic acid tert-butyl esteras beige solid; HPLC/MS 1.60 min (A), [M+H]+ 318.

¹H NMR (400 MHz, DMSO-d₆) δ 7.39 (d, J=8.8 Hz, 2H), 7.14 (d, J=8.8 Hz,2H), 4.06 (s, 2H), 3.76-3.62 (m, 4H), 1.44 (s, 9H).

The following compounds are prepared similarly

(4-Azido-benzyl)-dimethyl-amine; ¹H NMR (400 MHz, CDCl₃) δ 7.46 (d, 2H),6.99 (d, 2H), 3.38 (s, 2H), 2.25 (s, 6H).

(4-Azido-phenyl)-methanol; ¹H NMR (400 MHz, DMSO-d₆) δ 7.36 (d, 2H),7.07 (d, 2H), 5.25 t, 1H), 4.49 (d, 2H).

1-[2-(4-Azido-phenoxy)-ethyl]-pyrrolidine, brown oil; HPLC/MS 1.07 min(B), [M+H]⁺ 233.

4-[2-(4-Azido-phenoxy)-ethyl]-morpholine, brown oil; HPLC/MS 1.05 min(B), [M+H]⁺ 249.

¹H NMR (400 MHz, DMSO-d₆) δ 7.08-6.96 (m, 4H), 4.08 (t, J=5.8 Hz, 2H),3.56-3.60 (m, 4H), 2.68 (t, J=5.8 Hz, 2H), 2.44-2.49 (m, 2H).

4-(5-Azido-pyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butylester, brown solid; HPLC/MS 1.83 min (A), [M-^(t)bu]⁺ 250.

¹H NMR (300 MHz, DMSO-d₆) δ 8.29 (s, 2H), 3.72-3.65 (m, 4H), 3.46-3.36(m, 4H), 1.42 (s, 9H).

4-[2-(4-Azido-phenoxy)-ethyl]-piperazine-1-carboxylic acid tert-butylester, beige powder; HPLC/MS 1.30 min (A), [M+H]⁺ 348.

4-(4-Azido-phenyl)-piperazine-1-carboxylic acid tert-butyl ester, brownsolid; HPLC/MS 1.94 min (A), [M+H]⁺ 304.

4-(4-Azido-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester,brown oil; HPLC/MS 1.97 min (A), [M+H]⁺ 318.

4-(4-Azido-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester,brown oil; HPLC/MS 1.97 min (A), [M+H]⁺ 318.

(4-Azido-3-methyl-phenyl)-morpholin-4-yl-methanone, yellow resin;HPLC/MS 1.42 min (A), [M+H]⁺ 247.

5-Azido-1,2,3-trimethoxy-benzene, beige solid; HPLC/MS 1.56 min (A),[M+H]+ 210.

¹H NMR (400 MHz, DMSO-d₆) δ 6.42 (s, 2H), 3.80 (s, 6H), 3.64 (s, 3H).

(4-Azido-2-fluoro-phenyl)-morpholin-4-yl-methanone, light brown oil;HPLC/MS 1.31 min (A), [M+H]⁺ 251.

4-Azido-2-fluoro-N-methyl-benzamide, light brown oil; HPLC/MS 1.23 min(A), [M+H]⁺ 195.

4-[2-(3-Azido-phenoxy)-ethyl]-morpholine, brown oil; HPLC/MS 1.03 min(A), [M+H]⁺ 249.

3-(4-Azido-phenyl)-oxazolidin-2-one, pale brown powder; HPLC/MS 1.44 min(A), [M+H]⁺ 205. ¹H NMR (400 MHz, DMSO-d₆) δ 7.60 (d, J=9.0 Hz, 2H),7.15 (d, J=9.0 Hz, 2H), 4.59-4.33 (m, 2H), 4.10-4.00 (m, 2H).

2-(4-Azido-phenyl)-isothiazolidine 1,1-dioxide, beige powder; HPLC/MS1.47 min (A), [M+H]⁺ 239.

4-(4-Azido-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butylester, light yellow solid; UPLC/MS 0.90 min, [M+H]⁺ 268.

4-(4-Azido-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butylester, beige solid; HPLC/MS 1.93 min (A), [M+H]⁺ 275.

4-[2-(4-Azido-phenyl)-acetyl]-piperazine-1-carboxylic acid tert-butylester, light yellow solid; UPLC/MS 1.13 min, [M-^(t)Bu]⁺ 290. ¹H NMR(400 MHz, DMSO-d₆) δ 7.31-7.25 (m, 2H), 7.15-7.04 (m, 2H), 3.72 (s, 2H),3.50-3.42 (m, 4H), 3.30 -3.23 (m, 4H), 1.41 (s, 9H).

[2-(4-Azido-phenyl)-ethyl]-dimethyl-amine, red-brown oil; UPLC/MS 0.77min, [M+H]⁺ 191. ¹H NMR (500 MHz, DMSO-d₆) δ 7.27 (d, J=8.4 Hz, 2H),7.07-6.99 (m, 2H), 2.75-2.66 (m, 2H), 2.47-2.38 (m, 2H), 2.17 (s, 6H).

1-[2-(4-Azido-phenyl)-ethyl]-pyrrolidine, red-brown oil; UPLC/MS 0.78min, [M+H]⁺ 217. ¹H NMR (500 MHz, DMSO-d₆) δ 7.30-7.26 (m, 1H),7.06-7.01 (m, 1H), 2.73 (t, J=7.6 Hz, 1H), 2.60 (t, J=7.6 Hz, 1H),2.49-2.43 (m, 3H), 1.71-1.63 (m, 4H).

[2-(4-Azido-phenoxy)-ethyl]-diethyl-amine, brown liquid; HPLC/MS 1.08min (A), [M+H]⁺ 235.

Synthesis of 4-(4-azido-phenyl)-morpholin-3-one

A suspension of 4-(4-amino-phenyl)-morpholin-3-one (3.00 g, 15.6 mmol)in acetonitrile (35 ml) is cooled to 0° C. Then butyl nitrite (2.43 g,23.6 mmol) is added dropwise. The reaction mixture is stirred for 15minutes at 0° C. Then trimethylsilyl azide is added dropwise. Thereaction mixture is stirred for 20 hours at room temperature. Thereaction mixture is concentrated under reduced pressure and the residueis chromatographed on a silica gel column with cyclohexane/ethyl acetateas eluent to afford 4-(4-azido-phenyl)-morpholin-3-one as beige solid;HPLC/MS 1.21 min (B), [M+H]+ 219.

¹H NMR (300 MHz, DMSO-d₆) δ 7.45 (d, J=8.8 Hz, 2H), 7.16 (d, J=8.8 Hz,2H), 4.20 (s, 2H), 4.04-3.92 (m, 2H), 3.81-3.66 (m, 2H).

The following compounds are prepared similarly

4-(4-Azido-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester,beige solid; HPLC/MS 1.85 min (B), [M-^(t)bu]⁺ 277.

4-(4-Azido-2-fluoro-phenyl)-morpholin-3-one, yellow powder; HPLC/MS 1.27min (A), [M+H]+ 237.

¹H NMR (400 MHz, DMSO-d₆) δ 7.49 (t, J=8.4 Hz, 1H), 7.17 (dd, J=11.0,2.5 Hz, 1H), 7.05 (ddd, J=8.6, 2.5, 1.0 Hz, 1H), 4.22 (s, 2H), 4.03-3.82(m, 2H), 3.73-3.58 (m, 2H).

4-(5-Azido-pyridin-2-yl)-morpholin-3-one, yellow solid; HPLC/MS 1.15 min(A), [M+H]+ 220.

¹H NMR (400 MHz, DMSO-d₆) δ 8.27 (dd, J=2.9, 0.7 Hz, 1H), 8.05 (dd,J=8.9, 0.7 Hz, 1H), 7.69 (dd, J=8.9, 2.9 Hz, 1H), 4.27 (s, 2H),4.05-3.90 (m, 4H).

Synthesis of 2-(4-azido-phenyl)-propan-2-ol

To a suspension of 2-(4-bromo-phenyl)-propan-2-ol (1.00 g, 4.65 mmol),copper(I) iodide (177 mg, 0.93 mmol) and sodium(2R)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxy-ethanolatehydrate (100 mg, 0.46 mmol in a mixture of DMF (4 ml) and water (5 ml)are added sodium azide (605 mg, 9.3 mmol) andN,N′-dimethyl-ethane-1,2-diamine (123 mg, 1.39 mmol). The reactionmixture is stirred at room temperature for 19 hours. The reactionmixture is poured into 40 ml saturated aqueous sodium chloride solution.The mixture is extracted with ethyl acetate. The organic phase is driedover sodium sulfate and evaporated. The residue is chromatographed on asilica gel column with cyclohexane/ethyl acetate as eluent to afford2-(4-azido-phenyl)-propan-2-ol as light brown oil; HPLC/MS 1.47 min (B),[M-N₂-OH]⁺ 132.

¹H NMR (400 MHz, DMSO-d₆) δ 7.49 (d, J=8.4 Hz, 2H), 7.04 (d, J=8.4 Hz,2H), 5.01 (s, 1H), 1.41 (s, 6H).

The following compounds are prepared similarly

5-Azido-1H-indole, dark brown oil; HPLC/MS 1.46 min (B), [M+H]⁺ 159.

¹H NMR (300 MHz, DMSO-d₆) δ 11.19 (s, 1H), 7.43 (dt, J=8.6, 0.8 Hz, 1H),7.40 (t, J=2.8 Hz, 1H), 7.29 (dt, J=2.2, 0.7 Hz, 1H), 6.84 (dd, J=8.6,2.2 Hz, 1H), 6.42 (ddd, J=3.0, 2.0, 0.9 Hz, 1H).

(5-Azido-indol-1-yl)-acetic acid methyl ester, black gum; HPLC/MS 1.72min (A), [M+H]⁺ 231.

¹H NMR (400 MHz, DMSO-d₆) δ 7.47 (d, J=8.7 Hz, 1H), 7.41 (d, J=3.2 Hz,1H), 7.32 (d, J=2.1 Hz, 1H), 6.91 (d, J=2.2 Hz, 1H), 6.89 (d, J=2.2 Hz,1H), 6.47 (dd, J=3.2, 0.8 Hz, 2H), 5.16 (s, 1H), 3.69 (s, 3H).

Synthesis of (4-azido-phenyl)-morpholin-4-yl-methanone

To a solution of 4-azidobenzoic acid (2.50 g, 15.3 mmol), morpholine(1.35 ml, 15.5 mmol) and[dimethylamino(triazolo[4,5-b]pyridin-3-yloxy)methylene]-dimethyl-ammoniumhexafluorophosphate (HATU; 5.85 g, 15.4 mmol) in DMF (30 ml) is addedethyl-diisopropyl-amine (7.90 ml, 46.5 mmol) and the reaction mixture isstirred for 16 hours at room temperature. To the reaction mixture isadded ethyl acetate, saturated aqueous Na₂CO₃ solution and water. Theorganic phase is separated, washed with water, with 2 N aqueous HClsolution and saturated sodium chloride solution. The organic phase isdried over sodium sulfate and evaporated. The residue is chromatographedon a silica gel column with cyclohexane/ethyl acetate as eluent toafford (4-azido-phenyl)-morpholin-4-yl-methanone as colourless oil,which crystallizes on standing; HPLC/MS 1.27 min (A), [M+H]⁺ 233.

¹H NMR (400 MHz, DMSO-d₆) δ 7.48 (d, J=8.5 Hz, 2H), 7.20 (d, J=8.5 Hz,2H), 3.38-3-66 (m, 8H).

The following compounds are prepared similarly:

4-Azido-N,N-dimethylbenzamide, brown oil; HPLC/MS 2.24 min (A), [M+H]⁺191.

4-[(4-Azido-benzoyl)-methyl-amino]-piperidine-1-carboxylic acidtert-butyl ester, yellow oil; HPLC/MS 1.42 min (B), [M-^(t)bu]⁺304.

¹H NMR (400 MHz, DMSO-d₆) δ 7.44 (d, J=8.5 Hz, 2H), 7.24-7.08 (m, 1H),4.41 (m, 1H), 4.02 (m, 4H), 2.79 (s, 3H), 1.73-1.51 (m, 4H), 1.41 (s,9H).

4-Azido-N-(2-hydroxy-ethyl)-benzamide, white crystals; HPLC/MS 1.10 min(B), [M+H]⁺ 207.

4-Azido-N-(2-methoxy-ethyl)-benzamide.

[1-(4-Azido-benzoyl)-piperidin-4-yl]-carbamic acid tert-butyl ester,light yellow glass; HPLC/MS 1.45 min (B), [M+H]⁺ 346.

¹H NMR (400 MHz, DMSO-d₆) δ 7.40 (d, J=8.5 Hz, 1H), 7.17 (d, J=8.5 Hz,1H), 6.84 (d, J=7.8 Hz, 1H), 4.10-4.40 (m, 1H), 3.45-3.60 (m, 2H),2.85-3.15 (m, 2H), 1.65-1.85 (m, 2H), 1.38 (s, 9H), 1.20-1.40 (m, 2H).

4-(4-Azido-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester, lightyellow solid; HPLC/MS 1.49 min (B), [M-tbu]⁺276.

¹H NMR (300 MHz, DMSO-d₆) δ 7.47 (d, J=8.5 Hz, 2H), 7.19 (d, J=8.5 Hz,2H), 3.30-3.62 (m, 8H), 1.42 (s, 9H).

4-Azido-N-(2-morpholin-4-yl-ethyl)-benzamide, brown glass; HPLC/MS 0.98min (B), [M+H]⁺ 276.

4-(4-Azido-benzoylamino)-piperidine-1-carboxylic acid tert-butyl ester,light yellow solid; HPLC/MS 1.49 min (B), [M-tbu]⁺290.

¹H NMR (400 MHz, DMSO-d₆) δ 8.26 (d, J=7.8 Hz, 1H), 7.90 (d, J=8.6 Hz,2H), 7.20 (d, J=8.6 Hz, 2H), 3.90-4.03 (m, 3H), 2.77-2.94 (m, 2H),1.75-1.82 (m, 2H), 1.42 (s, 9H), 1.36-1.48 (m, 2H).

4-Azido-N-(1-methyl-piperidin-4-ylmethyl)-benzamide, light yellow oil;HPLC/MS 1.00 min (B), [M+H]⁺ 274.

(4-Azido-2-methyl-phenyl)-morpholin-4-yl-methanone, brown resin; HPLC/MS1.35 min (A), [M+H]⁺ 247

(4-Azido-phenyl)-[4-(3-methoxy-propyl)-piperazin-1-yl]-methanone, brownoil; HPLC/MS 1.00 min (A), [M+H]⁺ 304.

4-(3-Azido-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester, beigesolid; HPLC/MS 1.69 min (A), [M+H]⁺ 232.

4-(4-Azido-benzoyl)-1-methyl-piperazin-2-one, light yellow gum; HPLC/MS1.18 min (A), [M+H]⁺ 269.

¹H NMR (400 MHz, DMSO-d₆) δ 7.55-7.47 (m, 2H), 7.24-7.17 (m, 2H), 4.06(s, 1H), 3.87-3.54 (m, 2H), 3.36 (t, J=5.5 Hz, 1H), 2.86 (s, 3H).

(4-Azido-phenyl)-((R)-3-hydroxy-pyrrolidin-1-yl)-methanone, pale brownoil; HPLC/MS 1.16 min (A), [M+H]⁺ 233.

(4-Azido-phenyl)-((S)-3-hydroxy-pyrrolidin-1-yl)-methanone, pale brownoil; HPLC/MS 1.16 min (A), [M+H]⁺ 233.

(4-Azido-phenyl)-[1,3′]bipyrrolidinyl-1′-methanone, brown gum; HPLC/MS0.94 min (A), [M+H]⁺ 286.

1-(4-Azido-benzoyl)-4-methyl-[1,4]diazepan-5-one, yellow resin; UPLC/MS0.51 min, [M+H]⁺ 274.

Acetic acid 1-(4-azido-benzoyl)-piperidin-4-yl ester, yellow resin;HPLC/MS 1.48 min (A), [M+H]⁺ 289.

¹H NMR (400 MHz, DMSO-d₆) δ 7.38 (d, J=8.5 Hz, 2H), 7.16-6.99 (m, 2H),4.87 (tt, J=7.9, 3.8 Hz, 1H), 4.06-3.11 (m, 4H), 1.93 (s, 3H), 1.80 (bs,2H), 1.53 (bs, 2H).

Synthesis of 4-[2-(5-azido-indol-1-yl)-acetyl]-piperazine-1-carboxylicAcid Tert-Butyl Ester

4-[2-(5-azido-indol-1-yl)-acetyl]-piperazine-1-carboxylic acidtert-butyl ester, light beige solid; UPLC/MS 0.84 min, [M+H]⁺ 329.

Synthesis of 4-[2-(4-azido-phenoxy)-acetyl]-piperazine-1-carboxylic AcidTert-Butyl Ester

4-[2-(4-Azido-phenoxy)-acetyl]-piperazine-1-carboxylic acid tert-butylester, yellow solid; UPLC/MS 0.84 min, [M+H]⁺ 306.

Synthesis of 4-[2-(5-azido-indazol-1-yl)-acetyl]-piperazine-1-carboxylicAcid Tert-Butyl Ester

4-[2-(5-Azido-indazol-1-yl)-acetyl]-piperazine-1-carboxylic acidtert-butyl ester, purple solid, UPLC/MS 1.04 min, [M+H]⁺ 386.

Triazolyl-Acetic Acids

Synthesis of4-[4-(4-carboxymethyl-[1,2,3]triazol-1-yl)-benzoyl]-piperazine-1-carboxylicAcid Tert-Butyl Ester

To a suspension of copper(II) sulfate pentahydrate (86 mg, 0.54 mmol)and sodium(2R)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxy-ethanolatehydrate (116 mg, 0.54 mmol in a mixture of tert-butanol (10 ml) andwater (10 ml) are added 3-butynoic acid (451 mg, 5.37 mmol) and4-(4-azido-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (1.78g, 5.37 mmol). The reaction mixture is stirred at 80° C. for 19 hours.The reaction mixture is allowed to reach room temperature and pouredinto water. The resultant precipitate is filtered off, washed with waterand dried. The residue is triturated with tert-butyl methyl ether toafford4-[4-(4-carboxymethyl-[1,2,3]triazol-1-yl)-benzoyl]-piperazine-1-carboxylicacid tert-butyl ester as beige powder. A second crop can be obtained byextracting the filtrate with ethyl acetate. HPLC/MS 1.36 min (A), [M+H]⁺416. ¹H NMR (400 MHz, DMSO-d₆, d-TFA) δ 8.59 (s, 1H), 7.99 (d, J=8.5 Hz,2H), 7.64 (d, J=8.5 Hz, 2H), 3.84 (s, 2H), 3.35-3.75 (m, 8H), 1.45 (s,9H).

The following compounds are prepared similarly:

[1-(4-Fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-acetic acid, light brownsolid; HPLC/MS 1.18 min (B), [M+H]⁺ 222.

¹H NMR (400 MHz, DMSO-d₆, d-TFA) δ 8.48 (s, 1H), 7.86 (dd, J=9.0, 4.6Hz, 2H), 7.27 (t, J=8.7 Hz, 2H), 3.73 (s, 2H).

{1-[4-(Morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, beige solid; HPLC/MS 1.01 min (A), [M+H]⁺ 317.

¹H NMR (400 MHz, DMSO-d₆) δ 12.58 (s, 1H), 8.73 (s, 1H), 8.35-7.83 (m,2H), 7.86-7.52 (m, 2H), 3.80 (s, 2H), 3.48 (d, J=124.8 Hz, 9H).

4-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenyl]-piperazine-1-carboxylicacid tert-butyl ester, grey solid; HPLC/MS 1.51 min (A), [M+H]⁺ 388.

¹H NMR (400 MHz, DMSO-d₆, d-TFA) δ 8.56 (s, 1H), 7.85 (d, J=8.7 Hz, 2H),7.34 (d, J=8.8 Hz, 2H), 3.81 (s, 2H), 3.58-3.64 (m, 4H), 3.33-3-39 (m,4H), 1.46 (s, 9H).

{1-[4-(3-Oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, beige solid; HPLC/MS 1.06 min (A), [M+H]+ 303.

¹H NMR (400 MHz, DMSO-d₆, TFA-d1) δ 8.58 (s, 1H), 7.90 (d, J=8.8 Hz,2H), 7.60 (d, J=8.8 Hz, 2H), 4.21 (s, 2H), 3.99-3.95 (m, 2H), 3.82-3.71(m, 4H).

(1-{4-[4-(3-Methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-aceticacid, beige solid; HPLC/MS 0.86 min (A), [M+H]⁺ 388.

4-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenyl]-[1,4]diazepane-1-carboxylicacid tert-butyl ester, violet solid; HPLC/MS 1.52 min (A), [M+H]⁺ 402.

4-(3-Azido-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester, beigesolid; HPLC/MS 1.38 min (A), [M+H]⁺ 416.

{1-[4-(4-Methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, light yellow powder; UPLC/MS 0.40 min, [M+H]⁺ 344.

{1-[3-(2-Morpholin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, beige solid; HPLC/MS 0.88 min (A), [M+H]⁺ 333.

[1-(1-Methoxycarbonylmethyl-1H-indol-6-yl)-1H-[1,2,3]triazol-4-yl]-aceticacid, light brown solid; HPLC/MS 1.25 min (A), [M+H]⁺ 315.¹H NMR (400MHz, DMSO-d₆) δ 12.61 (bs, 1H), 8.56 (s, 1H), 8.03 (t, J=1.3 Hz, 1H),7.63-7.61 (m, 2H), 7.51 (d, J=3.2 Hz, 1H), 6.62 (d, J=3.2 Hz, 1H), 5.24(s, 2H), 3.78 (s, 2H), 3.71 (s, 3H).

{1-[4-((R)-3-Hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, dark brown oil; HPLC/MS 0.95 min (A), [M+H]⁺ 317.

{1-[4-((S)-3-Hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, dark brown oil; HPLC/MS 0.95 min (A), [M+H]⁺ 317.

{1-[4-(2-Oxo-oxazolidin-3-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown powder; HPLC/MS 1.08 min (A), [M+H]+ 289. ¹H NMR (400 MHz,DMSO-d₆, TFA-d₁) δ 8.63 (s, 1H), 8.19-7.87 (m, 2H), 7.87-7.70 (m, 2H),4.50 (m, 2H), 4.16 (m, 2H), 3.80 (s, 2H).

{1-[4-(1,1-Dioxo-isothiazolidin-2-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown powder; HPLC/MS 1.11 min (A), [M+H]⁺ 323.

{1-[4-(1,1-Dioxo-isothiazolidin-2-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown powder; HPLC/MS 1.11 min (A), [M+H]⁺ 323.

{1-[4-([1,3′]Bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown solid; HPLC/MS 0.84 min (A), [M+H]⁺ 370.

{1-[4-(4-Methyl-5-oxo-[1,4]diazepane-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown solid; UPLC/MS 0.40 min, [M+H]⁺ 358.

4-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-benzoyl]-piperidine-1-carboxylicacid tert-butyl ester, beige solid; HPLC/MS 1.57 min (A), [M+H]⁺ 415.

{1-[4-(4-Acetoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, beige solid; HPLC/MS 1.17 min (A), [M+H]⁺ 373.

{1-[4-(3-Acetoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, light brown foam; HPLC/MS 1.18 min (A), [M+H]⁺ 373.

4-{2-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenoxy]-ethyl}-piperazine-1-carboxylicacid tert-butyl ester, brown solid; HPLC/MS 1.10 min (A), [M+H]⁺ 432.

4-{3-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenoxy]-propyl}-piperazine-1-carboxylicacid tert-butyl ester, brown powder; HPLC/MS 1.12 min (A), [M+H]⁺ 446.

{1-[4-(3-Methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown foam; HPLC/MS 1.13 min (A), [M+H]⁺ 345.

{1-[3-([1,3′]Bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, light brown solid; HPLC/MS 0.84 min (A), [M+H]⁺ 370.

4-{2-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenoxy]-ethyl}-piperidine-1-carboxylicacid tert-butyl ester, brown oil, which crystallizes slowly; HPLC/MS1.73 min (A), [M+H]⁺ 431.

{1-[4-((R)-3-Methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, green resin; UPLC/MS 0.73 min, [M+H]⁺ 331.

{1-[4-((S)-3-Methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, green resin; UPLC/MS 0.73 min, [M+H]⁺ 331.

4-{2-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenyl]-acetyl}-piperazine-1-carboxylicacid tert-butyl ester, beige solid; UPLC/MS 0.92 min [M+H]⁺ 430.

{1-[4-(4-tert-Butoxycarbonylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, beige solid; UPLC/MS 0.90 min [M+H]⁺ 430. ¹H NMR (500 MHz,DMSO-d₆) δ 12.59 (s, 1H), 8.72 (s, 1H), 8.12-7.73 (m, 2H), 7.58 (d,J=8.5 Hz, 2H), 6.88 (d, J=7.7 Hz, 1H), 4.33 (bs, 1H), 3.80 (s, 2H), 3.55(bs, 2H), 3.14 (bs, 1H), 2.99 (bs, 1H), 1.77 (m, 2H), 1.40 (m, 11H).

4-{2-[5-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-indol-1-yl]-acetyl}-piperazine-1-carboxylicacid tert-butyl ester, beige solid; UPLC/MS 0.92 min, [M+H]⁺ 469.

4-{2-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenoxy]-acetyl}-piperazine-1-carboxylicacid tert-butyl ester, off-white solid; UPLC/MS 0.92 min, [M+H]⁺ 446.

{1-[4-(2-Dimethylamino-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, dark brown residue; UPLC/MS 0.63 min, [M+H]⁺ 275.

{1-[4-(2-Pyrrolidin-1-yl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, dark brown solid; UPLC/MS 0.65 min, [M+H]⁺ 301.

4-[4-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-phenyl]-3-oxo-piperazine-1-carboxylicacid tert-butyl ester, beige solid; HPLC/MS 1.34 min (A), [M+H]⁺ 402.

4-{2-[5-(4-Carboxymethyl-[1,2,3]triazol-1-yl)-indazol-1-yl]-acetyl}-piperazine-1-carboxylicacid tert-butyl ester, gray powder; UPLC/MS 0.88 min, [M+H]⁺ 470.

{1-[4-(2-Diethylamino-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown residue; HPLC/MS 0.91 min (A), [M+H]⁺ 391.

{1-[4-(2-Pyrrolidin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid, brown solid foam; HPLC/MS 0.89 min (A), [M+H]⁺ 317.

2-Aminobenzaldehydes Synthesis of 6-amino-2,3-difluoro-benzaldehyde

A suspension of 2,3-difluoro-6-aminobenzoic acid (1.00 g, 5.78 mmol) inTHF (30 ml) is cooled to 0° C. under nitrogen. Lithium aluminium hydride(1.0 M solution in THF, 8.7 ml, 8.7 mmol) is added dropwise within 30minutes. The reaction mixture is stirred for 1 hour at 0° C. and for 18hours at room temperature. The reaction mixture is quenched with waterand filtered over kieselguhr. The filtrate is concentrated in vacuo andthe residue is partitioned between water and ethyl acetate. The organicphase is dried over sodium sulfate and evaporated. The residue ischromatographed on a silica gel column with dichloromethane/methanol aseluent to afford (6-amino-2,3-difluoro-phenyl)-methanol as brown solid;HPLC/MS 0.99 min (A), [M+H]+ 160. ¹H NMR (400 MHz, DMSO-d₆) δ 7.01 (dt,J=10.6, 9.0 Hz, 1H), 6.42 (ddd, J=8.9, 4.1, 1.9 Hz, 1H), 5.13 (s, 2H),5.07 (t, J=5.5 Hz, 1H), 4.47 (dd, J=5.5, 2.3 Hz, 2H).

To a solution of (6-amino-2,3-difluoro-phenyl)-methanol (565 mg, 3.56mmol) in dichloromethane (8 ml) is added manganese dioxide (620 mg, 7.13mmol) and the reaction mixture is stirred at 80° C. for 3 hours. Thereaction mixture is allowed to reach room temperature and filtered overkieselguhr. The filtrate is evaporated to afford6-amino-2,3-difluoro-benzaldehyde as brown solid; HPLC/MS 1.44 min (A),[M+H]⁺ 158,

¹H NMR (400 MHz, DMSO-d₆) δ 10.16 (d, J=0.5 Hz, 1H), 7.44 (dt, J=10.5,9.3 Hz, 1H), 7.34 (s, 2H), 6.57 (dddd, J=9.4, 3.8, 2.0, 0.7 Hz, 1H).

The following compounds are prepared similarly

2-Amino-4,6-difluoro-benzaldehyde, dark red solid; HPLC/MS 1.47 min (A),[M+H]⁺ 158;

¹H NMR (400 MHz, DMSO-d₆) δ 10.08 (d, J=0.6 Hz, 1H), 7.73 (s, 2H),6.42-6.34 (m, 2H).

2-Amino-4,5-difluoro-benzaldehyde, dark brown residue; UPLC/MS 0.65 min,[M+H]⁺ 158.

¹H NMR (400 MHz, DMSO-d₆) δ 9.73 (s, 1H), 7.66 (dd, J=11.0, 9.1 Hz, 1H),7.23 (s, 2H), 6.70 (dd, J=13.2, 6.7 Hz, 1H).

2-Amino-4-trifluoromethyl-benzaldehyde, light orange solid; UPLC/MS 1.05min, [M+H]⁺ 190.

¹H NMR (500 MHz, DMSO-d₆) δ 9.95 (d, J=0.6 Hz, 1H), 7.79 (d, J=8.1 Hz,1H), 7.40 (s, 2H), 7.13 (s, 1H), 6.90 (dd, J=8.1, 1.7 Hz, 1H).

2-Amino-5-fluoro-4-methoxy-benzaldehyde, beige solid; HPLC/MS 1.31 min(A), [M+H]⁺ 170.

EXAMPLE 16-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A1”)

To a suspension of 3-ethynyl-6-fluoro-1H-quinolin-2-one (46.8 mg, 0.25mmol), copper(II) sulfate pentahydrate (4.0 mg, 0.03 mmol) and sodium(2R)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxy-ethanolatehydrate (5.4 mg, 0.03 mmol) in DMF (0.5 ml) is added(4-azido-phenyl)-morpholin-4-yl-methanone (65.0 mg, 0.28 mmol). Thereaction mixture is heated to 110° C. and stirred at this temperaturefor 22 hours. The reaction mixture is allowed to reach room temperature.Water is added and the resultant precipitate is filtered off, washedwith water and dried. The residue is chromatographed on a silica gelcolumn with dichloromethane/methanol as eluent to afford6-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas off-white powder; HPLC/MS 1.44 min (A), [M+H]+ 420.

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.10 (d, J=8.5 Hz, 2H), 7.80 (dd, J=9.3, 2.7 Hz, 1H), 7.65 (d, J=8.5 Hz,2H), 7.47 (dd, J=9.0, 2.7 Hz, 1H), 7.45-7.39 (m, 1H), 3.75-3.35 (m, 8H).

The following compounds are prepared similarly:

3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A2”)

beige solid, HPLC/MS 1.27 min (B), [M+H]⁺ 402; ¹H NMR (400 MHz, DMSO-d₆)δ 12.21 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H), 8.11 (d, J=8.2 Hz, 2H),7.92 (d, J=7.9 Hz, 1H), 7.67 (d, J=8.2 Hz, 2H), 7.57 (t, J=7.7 Hz, 1H),7.42 (d, J=8.3 Hz, 1H), 7.27 (t, J=7.5 Hz, 1H), 3.75-3.35 (m, 8H).

N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A3”)

beige powder; ¹H NMR (400 MHz, DMSO-d₆) δ 12.58 (s, 1H), 9.28 (s, 1H),8.87 (s, 1H), 8.59 (s, 1H), 8.38 (d, J=7.8 Hz, 1H), 8.09 (d, J=8.1 Hz,2H), 7.66 (d, J=8.1 Hz, 2H), 7.34 (t, J=6.3 Hz, 1H), 3.02 (s, 3H), 3.00(s, 3H).

N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A4”)

light yellow solid, HPLC/MS 1.28 min (B), [M+H]⁺ 360; ¹H NMR (400 MHz,DMSO-d₆) δ 12.22 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H), 8.14-8.04 (m, 2H),7.91 (dd, J=7.9, 1.4 Hz, 1H), 7.68-7.62 (m, 2H), 7.56 (ddd, J=8.5, 7.1,1.4 Hz, 1H), 7.41 (d, J=8.1 Hz, 1H), 7.26 (ddd, J=8.1, 7.2, 1.1 Hz, 1H),3.02 (s, 4H), 2.97 (s, 3H).

3-[1-(4-dimethylaminomethyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,8]naphthyridin-2-one(“A5”)

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.25 (br s, 1H), 8.83 (br s, 1H),8.57 (br s, 1H), 8.31 (d, 1H), 8.08 (d, 2H), 7.70 (d, 2H), 7.27 (br s,1H), 4.34 (s, 2H), 2.74 (s, 6H).

3-(1-phenyl-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one (“A6”)

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.22 (br s, 1H), 8.85 (br s, 1H),8.57 (brs, 1H), 8.35 (d, 1H), 7.98 (d, 1H), 7.59 (m, 2H), 7.50 (m, 2H),7.30 (br s, 1H).

3-[1-(4-hydroxymethyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,8]naphthyridin-2-one(“A7”)

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.20 (br s, 1H), 8.81 (br s, 1H),8.55 (br s, 1H), 8.30 (d, 1H), 7.80 (d, 1H), 5.70 (s, 2H), 7.47 (d, 2H),7.27 (d, 1H), 4.53 (s, 2H).

N-(2-hydroxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A8”)

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.31 (br s, 1H), 8.87 (br s, 1H),8.57 (br s, 1H), 8.36 (d, 1H), 8.13 (dd, 4H), 7.31 (br s, 1H), 3.51 (m,2H), 3.37 (m, 2H).

N-(2-methoxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A9”)

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.29 (br s, 1H), 8.83 (br s, 1H),8.55 (br s, 1H), 8.30 (br s, 1H), 8.05 (br s, 4H), 7.83 (br s, 0.5H),7.54 (br s, 0.5H), 7.26 (br s, 1H), 3.44 (s, 4H), 3.23 (s, 3H).

3-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A10”)

yellow-brown solid; HPLC/MS 1.43 min (B), [M+H]+ 319; ¹H NMR (400 MHz,DMSO-d₆) δ 12.19 (s, 1H), 9.09 (s, 1H), 8.82 (s, 1H), 7.95-7.86 (m, 3H),7.55 (ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.40 (d, J=8.1 Hz, 1H), 7.25 (ddd,J=8.2, 7.2, 1.1 Hz, 1H), 7.19-7.11 (m, 2H), 3.85 (s, 3H).

4-[4-(6-chloro-2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide (“A11”)

light brown solid; HPLC/MS 1.31 min (B), [M+H]⁺ 395; ¹H NMR (500 MHz,DMSO-d₆) δ 12.78 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.60 (d, J=2.5 Hz,1H), 8.55 (d, J=2.5 Hz, 1H), 8.08 (d, J=8.6 Hz, 2H), 7.65 (d, J=8.5 Hz,2H), 3.02 (s, 3H), 2.97 (s, 3H).

3-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one (“A12”)

light yellow solid; HPLC/MS 1.44 min (B), [M+H]⁺ 307; ¹H NMR (400 MHz,DMSO-d₆) δ 12.20 (s, 1H), 9.19 (s, 1H), 8.83 (s, 1H), 8.12-8.02 (m, 2H),7.90 (dd, J=7.9, 1.4 Hz, 1H), 7.56 (ddd, J=8.5, 7.2, 1.4 Hz, 1H),7.51-7.43 (m, 2H), 7.40 (dd, J=8.2, 1.0 Hz, 1H), 7.25 (ddd, J=8.1, 7.2,1.1 Hz, 1H).

3-[1-(2-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one (“A13”)

light yellow solid; HPLC/MS 1.43 min (B), [M+H]⁺ 307; ¹H NMR (400 MHz,DMSO-d₆) δ 12.20 (s, 1H), 9.06 (d, J=2.4 Hz, 1H), 8.85 (s, 1H), 7.95(td, J=7.9, 1.6 Hz, 1H), 7.91 (dd, J=8.0, 1.4 Hz, 1H), 7.68-7.52 (m,3H), 7.51-7.44 (m, 1H), 7.41 (dd, J=8.2, 1.0 Hz, 1H), 7.26 (ddd, J=8.1,7.2, 1.1 Hz, 1H).

3-{1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A14”)

light brown crystals; HPLC/MS 1.13 min (B), [M+H]+ 402; ¹H NMR (500 MHz,DMSO-d₆) δ 12.17 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 7.91-7.86 (m, 3H),7.55 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.40 (d, J=8.1 Hz, 1H), 7.28-7.22(m, 1H), 7.19-7.11 (m, 2H), 4.16 (t, J=5.9 Hz, 2H), 2.82 (t, J=5.8 Hz,2H), 2.56-2.52 (m, 3H), 1.72-1.68 (m, 4H).

N-(1-methyl-piperidin-4-ylmethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A15”)

brown solid; HPLC/MS 1.50 min (B), [M+H]+ 443; ¹H NMR (500 MHz, DMSO-d₆)δ 12.21 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.63 (t, J=5.8 Hz, 1H),8.13 (d, J=8.7 Hz, 2H), 8.08 (d, J=8.8 Hz, 2H), 7.91 (dd, J=8.0, 1.3 Hz,1H), 7.56 (ddd, J=8.4, 7.0, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.26(t, J=7.7 Hz, 1H), 3.19 (t, J=6.3 Hz, 2H), 2.84-2.74 (m, 2H), 2.19 (s,3H), 2.06-1.73 (m, 2H), 1.75-1.64 (m, 2H), 1.62-1.50 (m, 1H), 1.32-1.13(m, 2H).

4-[4-(6-methoxy-2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide(“A16”)

yellow solid; HPLC/MS 1.23 min (B), [M+H]⁺ 391; ¹H NMR (500 MHz,DMSO-d6) δ 12.51 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.36 (d, J=3.0 Hz,1H), 8.13-8.06 (m, 2H), 8.03 (d, J=3.0 Hz, 1H), 7.71-7.62 (m, 2H), 3.91(s, 3H), 3.03 (s, 3H), 2.98 (s, 3H).

4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-pyridine-2-carboxylicacid methyl ester (“A17”)

brown solid; HPLC/MS 1.30 min (B), [M+H]⁺ 348; ¹H NMR (400 MHz, DMSO-d₆)δ 12.23 (s, 1H), 9.52 (s, 1H), 8.91 (d, J=5.3 Hz, 1H), 8.87 (s, 1H),8.66 (d, J=2.1 Hz, 1H), 8.38 (dd, J=5.3, 2.2 Hz, 1H), 7.91 (d, J=7.6 Hz,1H), 7.57 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.26(t, J=7.4 Hz, 1H), 3.96 (s, 3H).

4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide (“A18”)

light yellow solid; HPLC/MS 1.31 min (B), [M+H]⁺ 378; ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H), 8.14-8.07 (m, 2H),7.81 (dd, J=9.2, 2.6 Hz, 1H), 7.70-7.63 (m, 2H), 7.52-7.40 (m, 2H), 3.03(s, 3H), 2.99 (s, 3H).

N-(2-hydroxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A19”)

light brown crystals; HPLC/MS 1.20 min (B), [M+H]⁺ 376; H NMR (400 MHz,DMSO-d₆) δ 12.20 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.60 (t, J=5.6 Hz,1H), 8.14 (d, J=8.8 Hz, 2H), 8.09 (d, J=8.8 Hz, 2H), 7.91 (d, J=7.1 Hz,OH), 7.56 (ddd, J=8.5, 7.2, 1.5 Hz, 1H), 7.41 (d, J=8.3 Hz, 1H),7.30-7.21 (m, 1H), 4.73 (t, J=5.6 Hz, 1H), 3.55 (q, J=6.0 Hz, 2H), 3.37(q, J=6.0 Hz, 2H).

3-[1-(1H-indol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one (“A20”)

brown solid; HPLC/MS 1.38 min (B), [M+H]⁺ 328; ¹H NMR (400 MHz, DMSO-d₆)δ 12.19 (s, 1H), 11.43 (s, 1H), 9.09 (s, 1H), 8.83 (s, 1H), 8.11 (s,1H), 7.91 (d, J=7.9 Hz, 1H), 7.70-7.50 (m, 4H), 7.41 (d, J=8.2 Hz, 1H),7.26 (t, J=7.5 Hz, 1H), 6.60 (s, 1H).

N-(2-morpholin-4-yl-ethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A21”)

light brown powder; HPLC/MS 1.10 min (B), [M+H]⁺ 445; ¹H NMR (500 MHz,DMSO-d₆) δ 12.21 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.58 (t, J=5.7 Hz,1H), 8.20-8.11 (m, 2H), 8.11-8.02 (m, 2H), 7.91 (dd, J=8.0, 1.4 Hz, 1H),7.56 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, OH), 7.26 (ddd,J=8.1, 7.2, 1.1 Hz, 1H), 3.60-3.56 (m, 4H), 3.43 (q, J=6.8 Hz, 2H),2.52-2.48 (m, 2H), 2.47-2.39 (m, 4H).

4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(1-methyl-piperidin-4-ylmethyl)-benzamide(“A22”)

red-brown solid; HPLC/MS 1.12 min (B), [M+H]⁺ 461; ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.31 (s, 1H), 8.85 (s, 1H), 8.62 (t, J=5.8 Hz,1H), 8.13 (d, J=8.8 Hz, 2H), 8.07 (d, J=8.8 Hz, 2H), 7.80 (dd, J=9.2,2.6 Hz, 1H), 7.53-7.34 (m, 2H), 3.18 (t, J=6.3 Hz, 2H), 2.81-2.71 (m,2H), 2.15 (s, 3H), 1.93-1.75 (m, 2H), 1.71-1.61 (m, 2H), 1.60-1.48 (m,1H), 1.26-1.14 (m, 2H).

3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic AcidMethyl Ester (“A23”)

light brown solid; HPLC/MS 1.45 min (B), [M+H]⁺ 347; ¹H NMR (400 MHz,DMSO-d₆) δ 12.21 (s, 1H), 9.31 (s, 1H), 8.85 (s, 1H), 8.50 (t, J=2.0 Hz,1H), 8.32 (dd, J=8.1, 1.4 Hz, 1H), 8.08 (dt, J=7.8, 1.3 Hz, 1H), 7.91(dd, J=8.0, 1.3 Hz, 1H), 7.78 (t, J=8.0 Hz, 1H), 7.56 (ddd, J=8.4, 7.2,1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.26 (t, J=7.4 Hz, 1H), 3.94 (s,3H).

3-[1-(3-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A24”)

yellow solid; HPLC/MS 1.45 min (B), [M+H]+ 319; ¹H NMR (400 MHz,DMSO-d₆) δ 12.17 (s, 1H), 9.22 (s, 1H), 8.82 (s, 1H), 7.90 (dd, J=8.1,1.4 Hz, 1H), 7.60-7.48 (m, 4H), 7.43-7.38 (m, 1H), 7.25 (ddd, J=8.1,7.2, 1.1 Hz, 1H), 7.08 (ddd, J=8.1, 2.4, 1.2 Hz, 1H), 3.89 (s, 3H).

3-{1-[4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A25”)

white solid; HPLC/MS 1.27 min (B), [M+H]⁺ 388; ¹H NMR (400 MHz, DMSO-d₆)δ 12.20 (s, 1H), 9.23 (s, 1H), 8.85 (s, 1H), 8.11-8.03 (m, 2H),7.95-7.88 (m, 1H), 7.74-7.65 (m, 2H), 7.57 (ddd, J=8.4, 7.1, 1.4 Hz,1H), 7.42 (d, J=8.2 Hz, 1H), 7.32-7.22 (m, 1H), 4.27 (s, 2H), 4.01-4.05(m, 2H), 3.87-3.82 (m, 2H).

3-{1-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A26”)

beige solid; HPLC/MS 1.08 min (B), [M+H]⁺ 418; ¹H NMR (400 MHz, DMSO-d₆)δ 12.17 (s, 1H), 9.09 (s, 1H), 8.82 (s, 1H), 7.92-7.87 (m, 3H), 7.56(ddd, J=8.4, 7.2, 1.4 Hz, 1H), 7.45-7.38 (m, 1H), 7.32-7.24 (m, 1H),7.22-7.13 (m, 2H), 4.20 (t, J=5.7 Hz, 2H), 3.65-3.57 (m, 4H), 2.75 (t,J=5.7 Hz, 2H), 2.52-2.49 (m, 4H).

3-(1-phenyl-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one (“A27”)

yellow crystals; HPLC/MS 1.43 min (B), [M+H]+ 289; ¹H NMR (500 MHz,DMSO-d₆) δ 12.19 (s, 1H), 9.19 (s, 1H), 8.83 (s, 1H), 8.03-7.97 (m, 2H),7.90 (dd, J=7.9, 1.3 Hz, 1H), 7.67-7.59 (m, 2H), 7.59-7.49 (m, 2H),7.43-7.39 (m, 1H), 7.26 (ddd, J=8.1, 7.2, 1.1 Hz, 1H).

3-[1-(3H-benzimidazol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A28”)

beige solid; HPLC/MS 1.09 min (B), [M+H]⁺ 329; ¹H NMR (400 MHz, DMSO-d₆,TFA-d₁) δ 9.67 (s, 1H), 9.32 (s, 1H), 8.82 (s, 1H), 8.47 (d, J=2.0 Hz,1H), 8.21 (dd, J=8.9, 2.0 Hz, 1H), 8.03 (d, J=8.9 Hz, 1H), 7.82 (dd,J=8.0, 1.3 Hz, 1H), 7.49 (ddd, J=8.4, 7.0, 1.4 Hz, 1H), 7.41 (d, J=8.2Hz, 1H), 7.27-7.12 (m, 1H).

3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one(“A29”)

beige solid; HPLC/MS 1.11 min (B), [M+H]+ 403; ¹H NMR (400 MHz, DMSO-d₆)δ 12.47 (s, 1H), 9.37 (s, 1H), 8.88 (s, 1H), 8.85 (bs, 1H), 8.48 (bs,1H), 8.17-8.06 (m, 2H), 7.91 (b, 1H), 7.75-7.60 (m, 2H), 3.80-3.35 (m,8H).

7-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A30”)

brown solid; HPLC/MS 1.24 min (B), [M+H]⁺ 417; ¹H NMR (500 MHz, DMSO-d₆)δ 12.46 (s, 1H), 9.24 (s, 1H), 8.82 (s, 1H), 8.24 (d, J=7.9 Hz, 1H),8.13-8.05 (m, 2H), 7.96 (s, 1H), 7.71-7.61 (m, 2H), 7.22 (d, J=7.9 Hz,1H), 3.64 (bs, 4H), 2.51 (bs, 4H), 1.25 (s, 3H).

6-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A31”)

brown solid, HPLC/MS 1.24 min (B), [M+H]⁺ 421; ¹H NMR (400 MHz, DMSO-d₆)δ 12.73 (s, 1H), 9.31 (s, 1H), 8.88 (s, 1H), 8.63 (d, J=2.9 Hz, 1H),8.36 (dd, J=8.7, 3.0 Hz, 1H), 8.17-8.04 (m, 2H), 7.77-7.55 (m, 2H),3.75-3.40 (m, 8H).

3-{1-[3-fluoro-4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A32”)

beige powder, HPLC/MS 1.42 min (A), [M+H]⁺ 406; ¹H NMR (400 MHz,DMSO-d₆) δ 12.21 (s, 1H), 9.32 (s, 1H), 8.84 (s, 1H), 8.12 (dd, J=11.0,2.4 Hz, 1H), 8.04-7.95 (m, 1H), 7.90 (dd, J=8.0, 1.4 Hz, 1H), 7.73 (t,J=8.4 Hz, 1H), 7.56 (ddd, J=8.4, 7.2, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz,1H), 7.26 (td, J=7.6, 1.1 Hz, 1H), 4.28 (s, 2H), 4.05-4.00 (m, 2H),3.81-3.65 (m, 2H).

6-fluoro-3-{1-[3-fluoro-4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A33”)

beige powder, HPLC/MS 1.47 min (A), [M+H]⁺ 424; ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.34 (s, 1H), 8.85 (s, 1H), 8.13 (dd, J=11.0,2.4 Hz, 1H), 8.01-7.95 (m, 1H), 7.80 (dd, J=9.3, 2.7 Hz, 1H), 7.73 (t,J=8.4 Hz, 1H), 7.52 -7.38 (m, 2H), 4.28 (s, 2H), 4.08-3.99 (m, 2H),3.90-3.66 (m, 2H).

3-{1-[6-(3-oxo-morpholin-4-yl)-pyridin-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A34”)

beige solid, HPLC/MS 1.41 min (A), [M+H]⁺ 389; ¹H NMR (400 MHz, DMSO-d₆)δ 12.21 (s, 1H), 9.32 (s, 1H), 9.11 (d, J=2.7 Hz, 1H), 8.86 (s, 1H),8.50 (dd, J=9.1, 2.8 Hz, 1H), 8.31 (d, J=9.0 Hz, 1H), 7.95-7.90 (m, 1H),7.57 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.42 (d, J=8.2 Hz, 1H), 7.31-7.24(m, 1H), 4.33 (s, 2H), 4.05 (s, 4H).

3-{1-[2-methyl-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A35”)

beige solid, HPLC/MS 1.40 min (A), [M+H]⁺ 416; ¹H NMR (300 MHz, DMSO-d₆)δ 12.16 (s, 1H), 8.92 (s, 1H), 8.84 (s, 1H), 7.89 (dd, J=8.0, 1.4 Hz,1H), 7.61 (d, J=8.1 Hz, 1H), 7.59-7.52 (m, 2H), 7.46 (dd, J=8.1, 1.9 Hz,1H), 7.40 (d, J=8.4 Hz, 1H), 7.26 (ddd, J=8.1, 7.2, 1.2 Hz, 1H),3.75-3.35 (m, 8H), 2.26 (s, 3H).

3-{1-[4-(1-hydroxy-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A36”)

light brown solid, HPLC/MS 1.47 min (A), [M+H]⁺ 347; ¹H NMR (400 MHz,DMSO-d₆) δ 12.18 (s, 1H), 9.15 (s, 1H), 8.82 (s, 1H), 7.93-7.88 (m, 3H),7.73-7.66 (m, 2H), 7.55 (ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.41 (dd, J=8.2,1.0 Hz, 1H), 7.25 (ddd, J=8.1, 7.2, 1.1 Hz, 1H), 5.17 (s, 1H), 1.49 (s,6H).

3-{1-[3-fluoro-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A37”)

yellow solid, HPLC/MS 1.45 min (A), [M+H]⁺ 420; ¹H NMR (400 MHz,DMSO-d₆) δ 12.22 (s, 1H), 9.35 (s, 1H), 8.86 (s, 1H), 8.12 (dd, J=10.4,2.0 Hz, 1H), 8.02 (dd, J=8.3, 2.0 Hz, 1H), 7.92 (dd, J=8.1, 1.4 Hz, 1H),7.68 (dd, J=8.3, 7.4 Hz, 1H), 7.58 (ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.42(d, J=8.2 Hz, 1H), 7.27 (ddd, J=8.1, 7.1, 1.1 Hz, 1H), 3.69 (s, 4H),3.61-3.56 (m, 2H), 3.35-3-30 (m, 2H).

3-[1-(3,4,5-trimethoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A38”)

beige solid, HPLC/MS 1.57 min (A), [M+H]+ 379; ¹H NMR (400 MHz, DMSO-d₆)δ 12.18 (s, 1H), 9.27 (s, 1H), 8.83 (s, 1H), 7.91 (dd, J=8.0, 1.4 Hz,1H), 7.56 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.42 (d, J=7.7 Hz, 1H), 7.31(s, 2H), 7.26 (ddd, J=8.2, 7.2, 1.1 Hz, 1H), 3.93 (s, 6H), 3.75 (s, 3H).

2-fluoro-N-methyl-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A39”)

beige solid, HPLC/MS 1.42 min (A), [M+H]+ 364; ¹H NMR (500 MHz, DMSO-d₆)δ 12.23 (s, 1H), 9.36 (s, 1H), 8.86 (s, 1H), 8.42-8.35 (m, 1H), 8.11(dd, J=11.3, 2.1 Hz, 1H), 8.00 (dd, J=8.4, 2.1 Hz, 1H), 7.92 (dd, J=8.0,1.3 Hz, 1H), 7.86 (t, J=8.1 Hz, 1H), 7.57 (ddd, J=8.4, 7.1, 1.4 Hz, 1H),7.42 (d, J=8.2 Hz, 1H), 7.33-7.23 (m, 1H), 2.83 (d, J=4.6 Hz, 3H).

3-{1-[3-methyl-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A40”)

yellow powder, HPLC/MS 1.43 min (A), [M+H]+ 416; ¹H NMR (400 MHz,DMSO-d₆) δ 12.21 (s, 1H), 9.25 (s, 1H), 8.85 (s, 1H), 8.00 (d, J=2.5 Hz,1H), 7.93-7.89 (m, 2H), 7.57 (ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.46-7.40(m, 2H), 7.27 (ddd, J=8.1, 7.2, 1.1 Hz, 1H), 3.70 (s, 4H), 3.55 (s, 2H),3.21 (s, 2H), 2.37 (s, 3H).

Example 23-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,6]naphthyridin-2-one(“A41”)

To a solution of 4-Amino-pyridine-3-carbaldehyde (61.1 mg, 0.50 mmol),{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid (158 mg, 0.50 mmol) and[dimethylamino-([1,2,3]triazolo[4,5-b]pyridin-3-yloxy)-methylene]-dimethyl-ammoniumhexafluorophosphate (HATU; 380 mg, 1.0 mmol) in DMF (1.3 ml) is addedN-ethyldiisopropylamine (257 μl, 1.5 mmol) and the reaction mixture isstirred for 17 hours at room temperature. Water is added to the reactionmixture. The resultant precipitate is filtered off, dried andchromatographed on a silica gel column with dichloromethane/methanol aseluent to afford3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,6]naphthyridin-2-oneas beige solid; HPLC/MS 1.02 min (A), [M+H]+ 403. ¹H NMR (400 MHz,DMSO-d₆) δ 12.46 (s, 1H), 9.28 (s, 1H), 9.10 (s, 1H), 8.93 (s, 1H), 8.52(d, J=5.7 Hz, 1H), 8.11 (d, J=8.6 Hz, 1H), 7.67 (d, J=8.6 Hz, 2H), 7.30(d, J=5.7 Hz, 1H), 3.35-3.75 (m, 8H).

The following compounds are prepared similarly:

N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-[1,7]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A42”)

brown powder, MS-ESI: [M+H]⁺ 361.

3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,8]naphthyridin-2-one (“A43”)

brown powder, HPLC/MS 1.34 min (B), [M+H]⁺ 289; H NMR (400 MHz, DMSO-d₆)δ 12.40 (s, 1H), 9.12 (s, 1H), 8.51 (dd, J=4.7, 1.7 Hz, 1H), 8.44 (s,1H), 8.42 (s, 1H), 8.11 (dd, J=7.8, 1.8 Hz, 1H), 7.96-7.82 (m, 2H),7.63-7.50 (m, 2H), 7.40-7.33 (m, 1H), 7.29 (dd, J=7.7, 4.7 Hz, 1H).

3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,7]naphthyridin-2-one (“A44”)

brown powder, HPLC/MS 1.21 min (B), [M+H]⁺ 289; ¹H NMR (400 MHz,DMSO-d₆) δ 12.27 (s, 1H), 9.19 (s, 1H), 8.69 (s, 1H), 8.50 (s, 1H), 8.44(s, 1H), 8.35 (d, J=5.2 Hz, 1H), 7.97-7.80 (m, 2H), 7.60 (d, J=5.0 Hz,1H), 7.58-7.50 (m, 2H), 7.42-7.26 (m, 1H).

3-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,6]naphthyridin-2-one(“A45”)

brown solid, HPLC/MS 1.09 min (B), [M+H]⁺ 308; ¹H NMR (500 MHz, DMSO-d₆,TFA-d₁) δ 9.44 (s, 1H), 9.17 (s, 1H), 9.07 (s, 1H), 8.61 (d, J=6.7 Hz,1H), 8.02 -7.92 (m, 2H), 7.70 (d, J=6.7 Hz, 1H), 7.31 (t, J=8.7 Hz, 2H).

3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,6]naphthyridin-2-one (“A46”)

beige powder, HPLC/MS 1.06 min (B), [M+H]⁺ 289; ¹H NMR (400 MHz,DMSO-d₆) δ 12.27 (s, 1H), 9.11 (s, 1H), 8.86 (d, J=0.7 Hz, 1H), 8.50 (s,1H), 8.46 (d, J=5.5 Hz, 2H), 7.91-7.85 (m, 2H), 7.57-7.50 (m, 2H),7.39-7.32 (m, 1H), 7.25 (d, J=5.7 Hz, 1H).

3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one“A47”)

beige solid, HPLC/MS 1.27 min (A), [M+H]⁺ 403; ¹H NMR (400 MHz, DMSO-d₆)δ 12.58 (s, 1H), 9.28 (s, 1H), 8.87 (s, 1H), 8.59 (dd, J=4.7, 1.8 Hz,1H), 8.38 (dd, J=7.8, 1.8 Hz, 1H), 8.11 (d, J=8.6 Hz, 2H), 7.78-7.60 (m,2H), 7.34 (dd, J=7.8, 4.7 Hz, 1H), 3.76-3.36 (m, 8H).

5-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A48”)

beige solid, HPLC/MS 1.45 min (A), [M+H]⁺ 420; 1H NMR (400 MHz, DMSO-d₆)δ 12.44 (s, 1H), 9.28 (s, 1H), 8.82 (s, 1H), 8.10 (d, J=8.6 Hz, 2H),7.66 (d, J=8.6 Hz, 2H), 7.57 (td, J=8.2, 6.0 Hz, 1H), 7.24 (d, J=8.4 Hz,1H), 7.18-7.05 (m, 1H), 3.75-3.35 (m, 8H).

3-{1-[4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one(“A49”)

beige solid, HPLC/MS 1.45 min (A), [M+H]⁺ 420; 1H NMR (400 MHz, DMSO-d₆)δ 12.44 (s, 1H), 9.28 (s, 1H), 8.82 (s, 1H), 8.10 (d, J=8.6 Hz, 2H),7.66 (d, J=8.6 Hz, 2H), 7.57 (td, J=8.2, 6.0 Hz, 1H), 7.24 (d, J=8.4 Hz,1H), 7.18-7.05 (m, 1H), 3.75-3.35 (m, 8H).

Example 33-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A50”)

A suspension of4-{4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperazine-1-carboxylicacid tert-butyl ester (43 mg, 0.09 mmol; synthesized in analogy toexample 1) in a 4 M solution of hydrochloric acid in dioxane (0.5 ml) isheated to 80° C. and stirred at this temperature in a closed reactionvial for 1 hour. The reaction mixture is allowed to reach roomtemperature. The solids are filtered off and washed with THF. Theresidue is treated with aqueous sodium carbonate solution. The solid isfiltered off, washed with water and ethanol and dried under vacuum toafford3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas light grey powder; HPLC/MS 1.07 min (B), [M+H]+ 401.

¹H NMR (400 MHz, DMSO-d₆) δ 12.21 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.08 (d, J=8.0 Hz, 2H), 7.90 (d, J=7.9 Hz, 1H), 7.61 (d, J=8.0 Hz, 2H),7.56 (t, J=7.6 Hz, 1H), 7.41 (d, J=8.3 Hz, 1H), 7.26 (t, J=7.5 Hz, 1H),3.65-3.35 (m, 4H), 2.8-2.6 (m, 4H).

The following compounds are prepared similarly:

4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N-piperidin-4-yl-benzamide(“A51”)

trifluoroacetate: ¹H NMR (400 MHz, DMSO-d₆) δ 12.62 (br s, 1H), 9.33 (brs, 1H), 8.87 (br s, 1H), 8.64-8.58 (m, 3H), 8.34 (m, 2H), 8.17 (d, 2H),8.10 (d, 2H), 7.34 (br s, 1H), 4.09 (br s, 1H), 3.06 (m, 2H), 2.02 (d,2H), 1.78-1.70 (m, 2H),

3-[1-(4-piperazin-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A52”)

light brown crystals; HPLC/MS 1.10 min (B), [M+H]⁺ 373; ¹H NMR (500 MHz,DMSO-d₆, TFA-d₁) δ 9.11 (s, 1H), 8.83 (s, 1H), 7.91-7.86 (m, 3H), 7.55(ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.45 (d, J=8.2 Hz, 1H), 7.28-7.19 (m,3H), 3.53-3.49 (m, 4H), 3.34-3.30 (m, 4H).

6-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A53”)

hydrochloride: light brown solid; HPLC/MS 1.07 min (B), [M+H]⁺ 419; 1HNMR (500 MHz, DMSO-d₆) δ 12.30 (s, 1H), 9.31 (s, 1H), 9.22 (bs, 2H),8.86 (s, 1H), 8.13 (d, J=8.6 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.72(d, J=8.6 Hz, 2H), 7.51-7.38 (m, 2H), 3.72 (bs, 4H), 3.20 (bs, 4H).

3-[1-(2-piperazin-1-yl-pyrimidin-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A54”)

hydrochloride: brown solid; HPLC/MS 1.14 min (A), [M+H]+ 375; ¹H NMR(400 MHz, DMSO-d₆) δ 12.20 (s, 1H), 9.18 (m, 3H), 8.99 (s, 2H), 8.82 (s,1H), 7.90 (d, J=7.8 Hz, 1H), 7.56 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.41(d, J=8.2 Hz, 1H), 7.30-7.21 (m, 1H), 4.06 (t, J=5.3 Hz, 4H), 3.26-3.19(m, 4H).

3-[1-(4-[1,4]diazepan-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A55”)

brown solid; HPLC/MS 1.22 min (A), [M+H]⁺ 387; ¹H NMR (500 MHz, DMSO-d₆)δ 12.13 (s, 1H), 8.95 (s, 1H), 8.79 (s, 1H), 7.88 (dd, J=8.0, 1.4 Hz,1H), 7.68 (d, J=9.1 Hz, 2H), 7.54 (ddd, J=8.5, 7.2, 1.4 Hz, 1H), 7.40(dd, J=8.2, 1.0 Hz, 1H), 7.24 (ddd, J=8.1, 7.2, 1.1 Hz, 1H), 6.85 (d,J=9.1 Hz, 2H), 3.60 (t, J=6.1 Hz, 2H), 3.52 (t, J=5.3 Hz, 2H), 2.95-2.85(m, 2H), 2.70-2.61 (m, 2H), 1.80 (p, J=6.1 Hz, 2H).

Example 46-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A56”)

To a solution of4-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperazine-1-carboxylicacid tert-butyl ester (52 mg, 0.10 mmol; prepared in analogy toexample 1) in formic acid (0.5 ml) is added formaldehyde (37% aqueoussolution, 22.5 μl, 0.30 mmol) and the reaction mixture is stirred for 1hour at 80° C. The reaction mixture is evaporated and the residue ispurified by preparative HPLC to afford6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas white powder; HPLC/MS 1.07 min (B), [M+H]⁺ 433.

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.10 (d, J=8.5 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.66-7.60 (m, 2H),7.50-7.40 (m, 2H), 3.78-3.50 (m, 4H), 2.47-2.26 (m, 4H), 2.22 (s, 3H).

The following compounds are prepared similarly:

3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A57”)

white powder; HPLC/MS 1.08 min (B), [M+H]+ 415; ¹H NMR (400 MHz,DMSO-d₆) δ 12.20 (s, 1H), 9.89 (s, 1H), 9.28 (s, 1H), 8.84 (s, 1H),8.28-8.07 (m, 2H), 7.90 (d, J=7.3 Hz, 1H), 7.72-7.68 (m, 2H), 7.56 (ddd,J=8.5, 7.1, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.26 (ddd, J=8.1, 7.2,1.1 Hz, 1H), 3.7-3.0 (m, 8H), 2.81 (s, 3H).

N-(1-Methyl-piperidin-4-yl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A58”)

formate: white solid; HPLC/MS 1.10 min (B), [M+H]⁺ 429; ¹H NMR (500 MHz,DMSO-d₆) δ 12.22 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.43 (d, J=7.7 Hz,1H), 8.20 (s, 2H), 8.14 (d, J=8.7 Hz, 2H), 8.11-8.07 (m, 2H), 7.92 (dd,J=8.0, 1.3 Hz, 1H), 7.57 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.42 (d, J=8.3Hz, 1H), 7.27 (td, J=7.6, 1.1 Hz, 1H), 3.79 (tdt, J=11.7, 8.3, 4.4 Hz,1H), 2.87-2.78 (m, 2H), 2.21 (s, 3H), 2.02 (td, J=11.8, 2.5 Hz, 2H),1.88-1.77 (m, 2H), 1.63 (qd, J=12.1, 3.8 Hz, 2H).

N-methyl-N-(1-methyl-piperidin-4-yl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A59”)

beige solid; HPLC/MS 1.09 min (B), [M+H]⁺ 443; ¹H NMR (400 MHz, DMSO-d₆)δ 12.20 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H), 8.12-8.04 (m, 2H), 7.90(dd, J=8.0, 1.4 Hz, 1H), 7.60 (d, J=8.2 Hz, 2H), 7.56 (ddd, J=8.5, 7.1,1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.32-7.22 (m, 1H), 4.4-4.2 (m, 1H),2.85 (s, 6H), 2.25-2.05 (m, 4H), 1.90-1.78 (m, 2H), 1.67-1.58 (m, 2H).

3-{1-[4-(1-methyl-piperidin-4-ylmethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A60”)

white solid; HPLC/MS 1.12 min (B), [M+H]⁺ 416; ¹H NMR (400 MHz, DMSO-d₆)δ 12.16 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 7.91-7.84 (m, 3H), 7.55(ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.40 (d, J=8.2 Hz, 1H), 7.33-7.22 (m,1H), 7.19-7.07 (m, 2H), 3.92 (d, J=6.0 Hz, 2H), 2.82-2.76 (m, 2H), 2.17(s, 3H), 1.92-1.84 (m, 2H), 1.81-1.70 (m, 3H), 1.45-1.26 (m, 2H).

3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A61”)

light yellow solid; HPLC/MS 1.06 min (B), [M+H]⁺ 443; ¹H NMR (400 MHz,DMSO-d₆) δ 12.19 (s, 1H), 9.25 (s, 1H), 8.84 (s, 1H), 8.11-8.03 (m, 2H),7.90 (dd, J=8.0, 1.4 Hz, 1H), 7.66-7.60 (m, 2H), 7.56 (ddd, J=8.5, 7.2,1.4 Hz, 1H), 7.41 (d, J=8.3 Hz, 1H), 7.26 (ddd, J=8.1, 7.1, 1.1 Hz, 1H),4.45 (bs, 1H), 3.64 (bs, 1H), 3.06 (bs, 1H), 2.89 (bs, 1H), 2.36 (tt,J=11.0, 3.6 Hz, 1H), 2.19 (s, 6H), 1.90-1.65 (m, 2H), 1.45-1.30 (m, 2H).

3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,6]naphthyridin-2-one(“A62”)

white solid; HPLC/MS 0.87 min (A), [M+H]⁺ 416; ¹H NMR (400 MHz, DMSO-d₆)δ 12.48 (s, 1H), 9.27 (s, 1H), 9.09 (bs, 1H), 8.92 (s, 1H), 8.52 (bs,1H), 8.15-8.04 (m, 2H), 7.70-7.56 (m, 2H), 7.29 (d, J=5.6 Hz, 1H),3.72-3.54 (m, 4H), 2.44-2.26 (m, 4H), 2.21 (s, 3H).

3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one(“A63”)

light brown solid; HPLC/MS 0.98 min (A), [M+H]⁺ 416; ¹H NMR (300 MHz,DMSO-d₆) δ 12.47 (bs, 1H), 9.34 (s, 1H), 8.86 (s, 1H), 8.75 (s, 1H),8.39 (d, J=5.2 Hz, 1H), 8.10 (d, J=8.6 Hz, 1H), 7.86 (d, J=5.2 Hz, 1H),7.63 (d, J=8.6 Hz, 1H), 3.5-3.2 (m, 4H), 2.42-2.29 (m, 4H), 2.21 (s,3H).

3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A64”)

beige solid; HPLC/MS 1.06 min (A), [M+H]⁺ 416; ¹H NMR (400 MHz, DMSO-d₆)δ 12.59 (s, 1H), 9.28 (s, 1H), 8.87 (s, 1H), 8.59 (dd, J=4.7, 1.8 Hz,1H), 8.38 (dd, J=7.9, 1.8 Hz, 1H), 8.10 (d, J=8.5 Hz, 1H), 7.64 (d,J=8.5 Hz, 1H), 7.34 (dd, J=7.7, 4.7 Hz, 1H), 3.7-3.3 (m, 4H), 2.45-2.25(m, 4H), 2.23 (s, 3H).

7-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A65”)

light yellow solid; HPLC/MS 1.11 min (A), [M+H]⁺ 430.

3-{1-[2-(4-methyl-piperazin-1-yl)-pyrimidin-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A66”)

beige solid; HPLC/MS 1.16 min (A), [M+H]⁺ 389; ¹H NMR (400 MHz, DMSO-d₆)δ 12.17 (s, 1H), 9.12 (s, 1H), 8.88 (s, 2H), 8.81 (s, 1H), 7.89 (dd,J=8.1, 1.3 Hz, 1H), 7.55 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.40 (d, J=8.3Hz, 1H), 7.28-7.23 (m, 1H), 3.88-3.77 (m, 4H), 2.45-2.35 (m, 4H), 2.24(s, 3H).

6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A67”)

white solid; HPLC/MS 1.09 min (A), [M+H]⁺ 434; ¹H NMR (400 MHz, DMSO-d₆)δ 12.73 (s, 1H), 9.30 (s, 1H), 8.87 (s, 1H), 8.61 (d, J=2.9 Hz, 1H),8.35 (dd, J=8.7, 2.9 Hz, 1H), 8.09 (d, J=8.6 Hz, 2H), 7.63 (d, J=8.5 Hz,2H), 3.74-3.30 (m, 4H), 2.44-2.26 (m, 4H), 2.21 (s, 3H).

3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A68”)

white solid; HPLC/MS 1.19 min (A), [M+H]⁺ 401; ¹H NMR (400 MHz, DMSO-d₆)δ 12.18 (s, 1H), 9.21 (s, 1H), 8.83 (s, 1H), 8.02 (d, J=8.9 Hz, 2H),7.90 (dd, J=8.1, 1.4 Hz, 1H), 7.67-7.58 (m, 2H), 7.55 (ddd, J=8.5, 7.1,1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.25 (td, J=7.5, 1.1 Hz, 1H),3.76-3.72 (m, 2H), 3.16 (s, 2H), 2.84-2.70 (m, 2H), 2.31 (s, 3H).

3-{1-[4-(4-methyl-[1,4]diazepan-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A69”)

beige solid; HPLC/MS 1.23 min (A), [M+H]+ 401; ¹H NMR (400 MHz, DMSO-d₆)δ 12.15 (s, 1H), 8.97 (s, 1H), 8.77 (s, 1H), 7.86 (dd, J=8.0, 1.4 Hz,1H), 7.68 (d, J=9.1 Hz, 2H), 7.52 (ddd, J=8.5, 7.1, 1.4 Hz, 1H), 7.39(d, J=8.2 Hz, 1H), 7.22 (ddd, J=8.1, 7.1, 1.2 Hz, 1H), 6.85 (d, J=9.2Hz, 2H), 3.65-3.55 (m, 2H), 3.50 (t, J=6.2 Hz, 2H), 2.70-2.58 (m, 2H),2.49-2.45 (m, 2H), 2.27 (s, 3H), 1.92 (p, J=5.9 Hz, 2H).

6-fluoro-3-{1-[4-(4-methyl-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A70”)

off-white solid; HPLC/MS 1.24 min (A), [M+H]⁺ 405; ¹H NMR (500 MHz,DMSO-d₆) δ 12.23 (s, 1H), 9.05 (s, 1H), 8.81 (s, 1H), 7.92-7.66 (m, 3H),7.49-7.37 (m, 2H), 7.11 (d, J=9.2 Hz, 2H), 3.24 (t, J=5.0 Hz, 4H), 2.47(t, J=5.0 Hz, 4H), 2.24 (s, 3H).

6-fluoro-3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A71”)

beige solid; HPLC/MS 1.19 min (A), [M+H]⁺ 419; ¹H NMR (500 MHz, DMSO-d₆)δ 12.26 (s, 1H), 9.23 (s, 1H), 8.84 (s, 1H), 8.03 (d, J=8.9 Hz, 2H),7.80 (dd, J=9.2, 2.6 Hz, 1H), 7.60 (d, J=8.9 Hz, 2H), 7.48-7.40 (m, 2H),3.74 (t, J=5.3 Hz, 2H), 3.16 (s, 2H), 2.76 (t, J=5.4 Hz, 2H), 2.31 (s,3H).

3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A72”)

white solid; HPLC/MS 1.20 min (A), [M+H]⁺ 431; ¹H NMR (400 MHz, DMSO-d₆)δ 12.16 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 7.92-7.85 (m, 3H), 7.55(ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.40 (d, J=8.1 Hz, 1H), 7.25 (ddd, J=8.1,7.1, 1.1 Hz, 1H), 7.20-7.12 (m, 2H), 4.16 (t, J=5.8 Hz, 2H), 2.72 (t,J=5.8 Hz, 2H), 2.54-2.50 (m, 4H), 2.33 (bs, 4H), 2.15 (s, 3H).

Example 53-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A73”) and3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A74”) a) Synthesis of4-{4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-benzoyl}-piperazine-1-carboxylicAcid Tert-Butyl Ester

b) Suzuki Reaction—Synthesis of4-{4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-pyrazol-1-yl]-benzoyl}-piperazine-1-carboxylicAcid Tert-Butyl Ester

3-(1-phenyl-1H-pyrazol-4-yl)-1H-quinolin-2-one (“A75”) is preparedsimilarly:

white powder; HPLC/MS 1.45 min (B), [M+H]⁺ 288; ¹H NMR (400 MHz,DMSO-d₆) δ 12.00 (s, 1H), 9.11 (s, 1H), 8.45 (s, 1H), 8.42 (s, 1H),7.91-7.85 (m, 2H), 7.68 (dd, J=7.9, 1.3 Hz, 1H), 7.56-7.51 (m, 2H), 7.49(ddd, J=8.4, 7.1, 1.5 Hz, 1H), 7.39-7.31 (m, 2H), 7.22 (ddd, J=8.2, 7.2,1.2 Hz, 1H).

c) Synthesis of3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A73”) and3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A74”)

“A73”: white solid; HPLC/MS 1.06 min (B), [M+H]+ 400; ¹H NMR (400 MHz,DMSO-d₆) δ 12.03 (s, 1H), 9.18 (s, 1H), 8.50 (s, 1H), 8.44 (s, 1H), 8.18(s, 1H), 7.99-7.93 (m, 2H), 7.70 (dd, J=8.0, 1.3 Hz, 1H), 7.59-7.54 (m,2H), 7.51 (ddd, J=8.5, 7.2, 1.5 Hz, 1H), 7.38 (d, J=8.2 Hz, 1H), 7.24(ddd, J=8.1, 7.2, 1.1 Hz, 1H), 3.46 (bs, 4H), 2.78 (bs, 4H).

“A74” formate: white solid; HPLC/MS 1.17 min (A), [M+H]+ 400; ¹H NMR(700 MHz, DMSO-d₆) δ 12.05 (s, 1H), 9.19 (s, 1H), 8.50 (s, 1H), 8.45 (s,1H), 8.00-7.93 (m, 2H), 7.69 (dd, J=8.0, 1.3 Hz, 1H), 7.60-7.53 (m, 2H),7.53 -7.48 (m, 1H), 7.37 (d, J=8.1 Hz, 1H), 7.23 (t, J=7.4 Hz, 1H), 3.65(bs, 2H), 3.40 (bs, 2H), 2.34 (bs, 4H), 2.21 (s, 3H).

Example 63-{1-[3-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A76”) a) Synthesis of3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic Acid

To a suspension of3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic acidmethyl ester (346 mg, 1.0 mmol) in THF/water (1:1, 4 ml) is addedlithium hydroxide (211 mg, 8.8 mmol) and the reaction mixture is stirredfor 2 hours at 65° C. After cooling to room temperature, 1 N aqueoushydrochloric acid is added until a pH of 1 is reached. The resultantprecipitate is filtered off, washed with water and dried under vacuum toafford3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic acidas olive green solid; HPLC/MS 1.31 min (B), [M+H]+ 333; ¹H NMR (400 MHz,DMSO-d₆) δ 13.40 (s, 1H), 12.22 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.47 (d, J=1.9 Hz, 1H), 8.31-8.24 (m, 2H), 8.06 (dt, J=7.6, 1.3 Hz, 1H),7.91 (d, J=7.5 Hz, 1H), 7.76 (t, J=7.9 Hz, 1H), 7.56 (ddd, J=8.5, 7.1,1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.29-7.23 (m, 1H).

4-[4-(2-Oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid (“A77”) is prepared similarly

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.31 (d, 1H), 8.86 (br s, 1H),8.54-8.53 (m, 3H), 8.34 (dd, 2H), 8.16 (m, 4H), 7.30 (m, 1H).

b) Synthesis of “A76”

To a solution of3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic acid(99.7 mg, 0.30 mmol), morpholine (26 μl, 0.39 mmol) and[dimethylamino(triazolo[4,5-b]pyridin-3-yloxy)methylene]-dimethyl-ammoniumhexafluorophosphate (HATU; 114 mg, 0.30 mmol) in DMF (0.6 ml) is addedethyl-diisopropyl-amine (153 μl, 0.90 mmol) and the reaction mixture isstirred for 16 hours at room temperature. The reaction mixture istreated with saturated aqueous Na₂CO₃ solution and water. The resultantprecipitate is filtered off, washed with water and dried under vacuum toafford3-{1-[3-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas off-white solid; HPLC/MS 1.28 min (B), [M+H]+ 402.

¹H NMR (500 MHz, DMSO-d₆) δ 12.20 (s, 1H), 9.28 (s, 1H), 8.84 (s, 1H),8.11 (ddd, J=8.1, 2.3, 1.0 Hz, 1H), 8.05 (t, J=1.9 Hz, 1H), 7.90 (dd,J=8.0, 1.3 Hz, 1H), 7.69 (t, J=7.9 Hz, 1H), 7.59-7.50 (m, 2H), 7.41 (d,J=8.2 Hz, 1H), 7.26 (td, J=7.5, 1.1 Hz, 1H), 3.74-3.34 (m, 8H).

Example 73-{1-[3-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A78”) and3-{1-[3-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A79”)

“A78”: light yellow solid; HPLC/MS 1.15 min (A), [M+H]+ 401.

¹H NMR (400 MHz, DMSO-d₆) δ 12.20 (s, 1H), 9.27 (s, 1H), 8.83 (s, 1H),8.12-8.05 (m, 1H), 8.01 (t, J=1.8 Hz, 1H), 7.89 (dd, J=8.0, 1.4 Hz, 1H),7.68 (t, J=7.9 Hz, 1H), 7.55 (ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.49 (dt,J=7.7, 1.3 Hz, 1H), 7.40 (d, J=8.2 Hz, 1H), 7.32-7.21 (m, 1H), 3.58 (bs,2H), 3.29 (bs, 2H), 2.81-2.62 (m, 4H).

“A79”: white solid; HPLC/MS 1.15 min (A), [M+H]+ 415.

¹H NMR (400 MHz, DMSO-d₆) δ 12.19 (s, 1H), 9.27 (s, 1H), 8.83 (s, 1H),8.10 (ddd, J=8.1, 2.3, 1.0 Hz, 1H), 8.02 (t, J=1.8 Hz, 1H), 7.90 (dd,J=8.0, 1.4 Hz, 1H), 7.68 (t, J=7.9 Hz, 1H), 7.56 (ddd, J=8.5, 7.1, 1.4Hz, 1H), 7.50 (dt, J=7.7, 1.2 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.25(ddd, J=8.2, 7.2, 1.1 Hz, 1H), 3.66 (bs, 2H), 3.38 (bs, 2H), 2.45-2.25(m, 4), 2.21 (s, 3H).

Example 83-[1-(4-isopropenyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A80”) and3-{1-[4-(1-methanesulfonyl-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A81”)

To a solution of3-{1-[4-(1-hydroxy-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(97.0 mg, 0.28 mmol) in dichloromethane (0.5 ml) is added sodiummethanesulfinate (62.6 mg, 0.61 mmol), followed by a solution oftrifluoroacetic acid (176 μl, 2.28 mmol) in dichloromethane (0.4 ml).The reaction mixture is stirred for 19 hours at room temperature. Thereaction mixture is diluted with dichloromethane and water. The organicphase is separated and the organic phase is extracted twice with water.The combined organic phases are dried over sodium sulfate andevaporated. The residue is chromatographed on a silica gel column withdichloromethane/methanol as eluent to afford two products:

“A80”:3-[1-(4-isopropenyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,white crystals; HPLC/MS 1.80 min (A), [M+H]+ 329;

¹H NMR (400 MHz, DMSO-d₆) δ 12.18 (s, 1H), 9.20 (s, 1H), 8.83 (s, 1H),8.03-7.95 (m, 2H), 7.90 (dd, J=8.0, 1.3 Hz, 1H), 7.78-7.70 (m, 2H), 7.56(ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.41 (d, J=8.1 Hz, 1H), 7.25 (ddd, J=8.1,7.1, 1.1 Hz, 1H), 5.56 (s, 1H), 5.23-5.20 (m, 1H), 2.18 (d, J=1.1 Hz,3H).

“A81”:3-{1-[4-(1-methanesulfonyl-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,white platelets; HPLC/MS 1.50 min (A), [M+H]⁺ 409;

¹H NMR (400 MHz, DMSO-d₆) δ 12.18 (s, 1H), 9.24 (s, 1H), 8.83 (s, 1H),8.12-8.02 (m, 2H), 7.90 (dd, J=8.1, 1.4 Hz, 1H), 7.87-7.81 (m, 2H), 7.56(ddd, J=8.4, 7.1, 1.4 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.26 (ddd, J=8.1,7.2, 1.1 Hz, 1H), 2.77 (s, 3H), 1.83 (s, 6H).

Example 97-chloro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A82”)

To a suspension of{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid (158 mg, 0.50 mmol) and 2-amino-4-chlorobenzaldehyde (77.8 mg, 0.5mmol) in acetic acid anhydride (0.5 ml) is added triethylamine (277 μl,2.0 mmol) and the reaction mixture is stirred for 18 hours at roomtemperature. The reaction mixture is diluted with ethyl acetate. Thesolid is filtered off and dried. The residue is treated with water. Thesolid is filtered off, washed with water and dried under vacuum toafford7-chloro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas beige powder; HPLC/MS 1.53 min (A), [M+H]⁺436.

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.26 (s, 1H), 8.85 (s, 1H),8.15-8.04 (m, 2H), 7.95 (d, J=8.5 Hz, 1H), 7.75-7.59 (m, 2H), 7.42 (d,J=2.1 Hz, 1H), 7.30 (dd, J=8.5, 2.0 Hz, 1H), 3.85-3.33 (m, 8H).

The following compounds are prepared similarly:

7-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A83”)

off-white crystals; HPLC/MS 1.44 min (A), [M+H]⁺ 420; ¹H NMR (400 MHz,DMSO-d₆) δ 12.27 (s, 1H), 9.24 (s, 1H), 8.86 (s, 1H), 8.17-8.04 (m, 2H),8.00 (dd, J=9.6, 6.1 Hz, 1H), 7.69-7.62 (m, 2H), 7.17-7.10 (m, 2H),3.80-3.35 (m, 8H).

7-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A84”)

beige solid; HPLC/MS 1.47 min (A), [M+H]⁺ 416; H NMR (500 MHz, DMSO-d₆)δ 12.13 (s, 1H), 9.24 (s, 1H), 8.80 (s, 1H), 8.13-8.07 (m, 2H), 7.79 (d,J=8.1 Hz, 1H), 7.70-7.63 (m, 2H), 7.20 (s, 1H), 7.11 (dd, J=8.1, 1.5 Hz,1H), 3.75-3.35 (m, 8H), 2.43 (s, 3H).

3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,5]naphthyridin-2-one(“A85”)

light yellow crystals; HPLC/MS 1.20 min (A), [M+H]+ 403; ¹H NMR (700MHz, DMSO-d₆) δ 12.40 (s, 1H), 9.34 (s, 1H), 8.76 (s, 1H), 8.58 (dd,J=4.5, 1.4 Hz, 1H), 8.11 (d, J=8.6 Hz, 2H), 7.78 (dd, J=8.3, 1.4 Hz,1H), 7.66 (d, J=8.5 Hz, 2H), 7.58 (dd, J=8.3, 4.4 Hz, 1H), 3.65 (bs,4H), 3.40 (bs, 4H).

6-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A86”)

beige solid; HPLC/MS 1.23 min (A), [M+H]⁺ 491; ¹H NMR (400 MHz, DMSO-d₆)δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H), 8.08 (d, J=8.6 Hz, 2H),7.80 (dd, J=9.1, 2.6 Hz, 1H), 7.62 (d, J=8.6 Hz, 2H), 7.50-7.37 (m, 2H),3.75-3.30 (m, 4H), 3.35 (t, J=6.4 Hz, 2H), 3.22 (s, 3H), 2.47-2.32 (m,6H), 1.67 (p, J=6.7 Hz, 2H).

5-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A87”)

off-white solid; HPLC/MS 1.25 min (A), [M+H]+ 491; ¹H NMR (400 MHz,DMSO-d₆) δ 12.43 (s, 1H), 9.28 (s, 1H), 8.82 (s, 1H), 8.09 (d, J=8.6 Hz,2H), 7.62 (d, J=8.6 Hz, 2H), 7.57 (td, J=8.2, 6.1 Hz, 1H), 7.24 (d,J=8.4 Hz, 1H), 7.11 (ddd, J=10.1, 8.1, 0.9 Hz, 1H), 3.70-3.30 (m, 4H),3.35 (t, J=6.4 Hz, 2H), 3.22 (s, 3H), 2.40 (bs, 4H), 2.36 (t, J=7.3 Hz,2H), 1.78-1.57 (m, 2H).

6-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one(“A88”)

beige solid; HPLC/MS 1.14 min (A), [M+H]⁺ 492; ¹H NMR (400 MHz, DMSO-d₆)δ 12.70 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H), 8.61 (d, J=2.9 Hz, 1H),8.35 (dd, J=8.7, 3.0 Hz, 1H), 8.09 (d, J=8.6 Hz, 2H), 7.63 (d, J=8.6 Hz,2H), 3.75-3.30 (m, 4H), 3.35 (t, J=6.4 Hz, 2H), 3.22 (s, 3H), 2.39 (bs,4H) 2.36 (t, J=7.3 Hz, 2H), 1.67 (p, J=6.6 Hz, 2H).

3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one(“A89”)

white solid; HPLC/MS 1.08 min (A), [M+H]⁺ 474; ¹H NMR (500 MHz, DMSO-d₆)δ 12.58 (s, 1H), 9.27 (s, 1H), 8.86 (s, 1H), 8.57 (dd, J=4.7, 1.8 Hz,1H), 8.36 (dd, J=7.8, 1.8 Hz, 1H), 8.08 (d, J=8.5 Hz, 2H), 7.63 (d,J=8.5 Hz, 2H), 7.33 (dd, J=7.7, 4.7 Hz, 1H), 3.70-3.32 (m, 4H), 3.35 (t,J=6.4 Hz, 2H), 3.22 (s, 3H), 2.40 (bs, 4H), 2.36 (t, J=7.3 Hz, 2H), 1.67(m, 2H).

5,7-difluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A90”)

beige solid; HPLC/MS 1.51 min (A), [M+H]⁺ 438; ¹H NMR (500 MHz, DMSO-d₆)δ 12.54 (s, 1H), 9.28 (s, 1H), 8.77 (s, 1H), 8.11 (d, J=8.6 Hz, 2H),7.67 (d, J=8.6 Hz, 2H), 7.24 (td, J=9.9, 2.4 Hz, 1H), 7.03 (dd, J=9.9,2.1 Hz, 1H), 3.75-3.35 (m, 8H).

7-bromo-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A91”)

beige solid; HPLC/MS 1.56 min (A), [M+H]+ 482; ¹H NMR (400 MHz, DMSO-d₆)δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H), 8.15-8.07 (m, 2H), 7.89 (d,J=8.5 Hz, 1H), 7.72-7.63 (m, 2H), 7.59 (d, J=1.9 Hz, 1H), 7.44 (dd,J=8.4, 1.9 Hz, 1H), 3.74-3.38 (m, 8H).

6-fluoro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A92”)

off-white powder; UPLC/MS 0.62 min, [M+H]⁺ 447; ¹H NMR (400 MHz,DMSO-d₆) δ 12.27 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H), 8.15-8.07 (m, 2H),7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.75-7.66 (m, 2H), 7.52-7.38 (m, 2H), 4.12(bs, 2H), 3.94-3.58 (m, 2H), 3.40 (t, J=5.5 Hz, 2H), 2.89 (s, 3H).

7-methoxy-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A93”)

beige powder; UPLC/MS 0.66 min, [M+H]⁺ 432; ¹H NMR (400 MHz, DMSO-d₆) δ12.06 (s, 1H), 9.19 (s, 1H), 8.76 (s, 1H), 8.13-8.04 (m, 2H), 7.82 (d,J=8.3 Hz, 1H), 7.73-7.62 (m, 2H), 6.96-6.83 (m, 2H), 3.85 (s, 3H),3.72-3.38 (m, 8H).

6-{1-[4-(Morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-8H-pyrido[2,3-d]pyrimidin-7-one(“A94”

yellow solid; HPLC/MS 1.15 min (A), [M+H]+ 404; ¹H NMR (400 MHz,DMSO-d₆) δ 12.97 (s, 1H), 9.30 (s, 1H), 9.29 (s, 1H), 9.03 (s, 1H), 8.91(s, 1H), 8.15-8.10 (m, 2H), 7.71-7.66 (m, 3H), 3.64 (s, 16H).

6-fluoro-3-{1-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A94a”)

light beige solid; HPLC/MS 1.24 min (A), [M+H]⁺ 436; ¹H NMR (400 MHz,DMSO-d₆) δ 12.25 (s, 1H), 9.25 (s, 1H), 8.83 (s, 1H), 7.79 (dd, J=9.2,2.6 Hz, 1H), 7.59-7.54 (m, 2H), 7.50 (t, J=8.4 Hz, 1H), 7.46-7.39 (m,2H), 7.08 (ddd, J=8.2, 2.4, 1.2 Hz, 1H), 4.24 (t, J=5.7 Hz, 2H),3.64-3.55 (m, 4H), 2.74 (t, J=5.7 Hz, 2H), 2.53-2.49 (m, 4H).

5,7-difluoro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A95”)

off-white powder; UPLC/MS 0.66 min, [M+H]⁺ 465; ¹H NMR (400 MHz,DMSO-d₆) δ 12.50 (s, 1H), 9.28 (s, 1H), 8.75 (s, 1H), 8.27-8.03 (m, 2H),7.81-7.59 (m, 2H), 7.21 (td, J=9.9, 2.4 Hz, 1H), 7.01 (dd, J=9.9, 2.3Hz, 1H), 4.13 (bs, 2H), 3.94-3.60 (m, 2H), 3.44-3.36 (m, 2H), 2.89 (s,3H).

6-chloro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A96”)

off-white powder; UPLC/MS 0.67 min, [M+H]+ 463; ¹H NMR (400 MHz,DMSO-d₆) δ 12.32 (s, 1H), 9.29 (s, 1H), 8.84 (s, 1H), 8.16-8.08 (m, 2H),8.05 (d, J=2.3 Hz, 1H), 7.74-7.67 (m, 2H), 7.59 (dd, J=8.8, 2.4 Hz, 1H),7.41 (d, J=8.8 Hz, 1H), 4.13 (bs, 2H), 3.94-3.60 (m, 2H), 3.40 (t, J=5.4Hz, 2H), 2.89 (s, 3H).

7-chloro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A97”)

off-white powder; UPLC/MS 0.67 min, [M+H]⁺ 463; ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.27 (s, 1H), 8.86 (s, 1H), 8.16-8.08 (m, 2H),7.95 (d, J=8.5 Hz, 1H), 7.77-7.66 (m, 2H), 7.42 (d, J=2.0 Hz, 1H), 7.30(dd, J=8.4, 2.1 Hz, 1H), 4.12 (bs, 2H), 3.94-3.60 (m, 2H), 3.40 (t,J=5.5 Hz, 2H), 2.89 (s, 3H).

6-fluoro-3-{1-[4-(2-oxo-oxazolidin-3-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A98”)

off-white powder; HPLC/MS 1.51 min (A), [M+H]⁺ 392; ¹H NMR (400 MHz,DMSO-d₆) δ 12.26 (s, 1H), 9.19 (s, 1H), 8.83 (s, 1H), 8.23-7.95 (m, 2H),7.90-7.77 (m, 3H), 7.51-7.34 (m, 2H), 4.49 (m, 2H), 4.15 (m, 2H).

3-{1-[4-(1,1-dioxo-116-isothiazolidin-2-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A99”)

pale brown powder; HPLC/MS 1.53 min (A), [M+H]+ 426; ¹H NMR (500 MHz,DMSO-d₆) δ 12.26 (s, 1H), 9.18 (s, 1H), 8.84 (s, 1H), 8.13-7.94 (m, 2H),7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.48-7.37 (m, 4H), 3.84 (t, J=6.5 Hz, 2H),3.58 (t, J=7.4 Hz, 2H), 2.45 (p, J=6.8 Hz, 2H).

3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A100”)

beige solid; HPLC/MS 1.20 min (A), [M+H]⁺ 473; ¹H NMR (700 MHz, DMSO-d₆,TFA-d₁) δ 9.32 (s, 1H), 8.87 (s, 1H), 8.12 (d, J=8.3 Hz, 2H), 7.81 (d,J=8.1 Hz, 2H), 7.65 (dd, J=9.0, 2.8 Hz, 1H), 7.50 (dd, J=9.0, 4.7 Hz,1H), 7.37 (td, J=8.7, 2.8 Hz, 1H), 4.18-3.46 (m, 7H), 3.33-3.01 (m, 2H),2.51-1.95 (m, 6H).

3-(1-{4-[2-(4-acetyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-6-fluoro-1H-quinolin-2-one(“A100a”)

brown solid; HPLC/MS 1.21 min (A), [M+H]⁺ 477; ¹H NMR (500 MHz, DMSO-d₆)δ 12.24 (s, 1H), 9.11 (s, 1H), 8.82 (s, 1H), 7.93-7.85 (m, 2H), 7.79(dd, J=9.2, 2.7 Hz, 1H), 7.49-7.38 (m, 2H), 7.21-7.12 (m, 2H), 4.19 (t,J=5.7 Hz, 2H), 3.50-3.39 (m, 4H), 2.77 (t, J=5.7 Hz, 2H), 2.52 (m, 2H),2.45 (m, 2H), 1.99 (s, 3H).

3-(1-{4-[2-(4-acetyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-6,7-difluoro-1H-quinolin-2-one(“A101”)

brown solid; HPLC/MS 1.25 min (A), [M+H]⁺ 495; ¹H NMR (500 MHz, DMSO-d₆)δ 12.29 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 8.07 (dd, J=11.0, 8.6 Hz,1H), 7.96-7.82 (m, 2H), 7.32 (dd, J=11.4, 7.0 Hz, 1H), 7.24-7.10 (m,2H), 4.19 (t, J=5.7 Hz, 2H), 3.50-3.38 (m, 4H), 2.77 (t, J=5.7 Hz, 2H),2.52 (m, 2H), 2.45 (t, J=5.2 Hz, 2H), 1.99 (s, 3H).

Acetic Acid1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperidin-4-ylEster (“A102”)

beige solid; HPLC/MS 1.55 min (A), [M+H]⁺ 476.

acetic acid1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperidin-3-ylester (“A103”)

off-white solid; HPLC/MS 1.55 min (A), [M+H]⁺ 476.

3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A104”)

brown solid; HPLC/MS 1.24 min (A), [M+H]⁺ 491.

3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-5,7-difluoro-1H-quinolin-2-one(“A105”)

beige solid; HPLC/MS 1.25 min (A), [M+H]⁺ 491.

6-fluoro-3-{1-[4-(3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A106”)

light brown solid; HPLC/MS 1.52 min (A), [M+H]⁺ 448.

3-{1-[3-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A107”)

brown solid; HPLC/MS 1.20 min (A), [M+H]⁺ 473.

3-{1-[3-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A108”)

brown solid; HPLC/MS 1.24 min (A), [M+H]⁺ 491.

6,7-difluoro-3-{1-[4-(3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A109”)

brown solid; HPLC/MS 1.56 min (A), [M+H]⁺ 466.

6-fluoro-3-{1-[4-(4-methyl-5-oxo-[1,4]diazepane-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A110”)

brown solid; UPLC/MS 0.89 min, [M+H]+ 461.

6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A111”)

off-white solid; UPLC/MS 0.94 min, [M+H]⁺ 434.

6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A112”)

off-white solid; UPLC/MS 0.94 min, [M+H]⁺ 434.

6,7-difluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A113”)

off-white solid; UPLC/MS 0.96 min, [M+H]⁺ 452.

6,7-difluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A114”)

off-white solid; UPLC/MS 0.96 min, [M+H]⁺ 452.

3-{1-[4-(2-dimethylamino-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A115”)

beige solid; UPLC/MS 0.48 min, [M+H]⁺ 396. ¹H NMR (300 MHz, DMSO-d₆) δ12.31 (s, 1H), 9.15 (s, 1H), 8.83 (s, 1H), 8.08 (dd, J=11.1, 8.6 Hz,1H), 7.93-7.84 (m, 2H), 7.50-7.43 (m, 2H), 7.33 (dd, J=11.5, 7.1 Hz,1H), 2.81 (t, J=7.5 Hz, 2H), 2.53 (t, J=7.5 Hz, 2H), 2.21 (s, 6H).

6,7-difluoro-3-{1-[4-(2-pyrrolidin-1-yl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A115a”)

beige solid; UPLC/MS 0.49 min, [M+H]+ 396. ¹H NMR (300 MHz, DMSO-d₆) δ12.31 (s, 1H), 9.15 (s, 1H), 8.83 (s, 1H), 8.08 (dd, J=11.1, 8.6 Hz,1H), 7.89 (d, J=8.5 Hz, 2H), 7.47 (d, J=8.5 Hz, 2H), 7.33 (dd, J=11.5,7.1 Hz, 1H), 2.81 (t, J=7.5 Hz, 2H), 2.56-2.49 (m, 6H), 2.21 (s, 4H).

3-{1-[4-(2-diethylamino-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A116”)

beige solid; HPLC/MS 1.31 min (A), [M+H]⁺ 440; ¹H NMR (500 MHz, DMSO-d₆)δ 12.29 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 8.07 (dd, J=11.0, 8.5 Hz,1H), 7.96-7.82 (m, 2H), 7.31 (dd, J=11.4, 7.0 Hz, 1H), 7.19-7.07 (m,2H), 4.10 (t, J=6.1 Hz, 2H), 2.81 (t, J=6.1 Hz, 2H), 2.57 (q, J=7.1 Hz,4H), 0.99 (t, J=7.1 Hz, 6H).

6,7-difluoro-3-{1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A186”)

Beige solid; HPLC/MS 1.28 min (A), [M+H]⁺ 438; ¹H NMR (500 MHz, DMSO-d₆)δ 12.29 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 8.06 (dd, J=11.0, 8.6 Hz,1H), 7.87 (d, J=9.0 Hz, 2H), 7.31 (dd, J=11.4, 7.1 Hz, 1H), 7.15 (d,J=9.0 Hz, 2H), 4.16 (t, J=5.9 Hz, 2H), 2.83 (t, J=5.8 Hz, 2H), 2.58-2.53(m, 4H), 1.74-1.66 (m, 4H).

N-{4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-N-methyl-acetamide(“A352”)

HPLC/MS 1.50 min (A), [M+H]⁺ 396;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.24 (s, 1H), 8.84 (s, 1H),8.12-8.05 (m, 3H), 7.68-7.54 (m, 2H), 7.33 (dd, J=11.5, 7.1 Hz, 1H),3.24 (bs, 3H), 1.90 (bs, 3H).

N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-N-methyl-acetamide(“A353”)

HPLC/MS 1.45 min (A), [M+H]⁺ 378;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.07 (d, J=8.2 Hz, 2H), 7.80 (dd, J=9.3, 2.6 Hz, 1H), 7.59 (d, J=8.5 Hz,2H), 7.53 -7.38 (m, 2H), 3.24 (bs, 3H), 1.90 (bs, 3H).

6-fluoro-3-[1-(2-methyl-1-oxo-2,3-dihydro-1H-isoindol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A354”)

UPLC/MS 0.66 min, [M+H]⁺ 376;

¹H NMR (400 MHz, DMSO-d₆) δ 12.30 (s, 1H), 9.34 (s, 1H), 8.88 (s, 1H),8.31 (d, J=1.9 Hz, 1H), 8.15 (dd, J=8.2, 2.0 Hz, 1H), 7.87 (d, J=8.2 Hz,1H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.54-7.30 (m, 2H), 3.13 (s, 3H), 2.55(s, 2H).

6-Fluoro-3-{1-[4-((trans)-3-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A355”)

HPLC/MS 1.73 min (A), [M+H]⁺ 421;

¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H), 9.09 (s, 1H), 8.82 (s, 1H),7.92-7.83 (m, 2H), 7.79 (dd, J=9.1, 2.6 Hz, 1H), 7.51-7.37 (m, 2H),7.15-7.00 (m, 2H), 4.85 (tt, J=7.2, 3.4 Hz, 1H), 3.83 (p, J=4.7 Hz, 1H),3.20 (s, 3H), 2.39 (dt, J=14.1, 7.0 Hz, 1H), 2.07-1.96 (m, 1H),1.90-1.74 (m, 2H), 1.69 (dt, J=14.4, 3.9 Hz, 1H).

6-chloro-3-{1-[4-((1S,3R)-3-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A356”)

HPLC/MS 1.83 min (A), [M+H]⁺ 437;

¹H NMR (500 MHz, DMSO-d₆) δ 12.30 (s, 1H), 9.10 (s, 1H), 8.82 (s, 1H),8.05 (d, J=2.4 Hz, 1H), 7.87 (d, J=9.0 Hz, 2H), 7.58 (dd, J=8.8, 2.4 Hz,1H), 7.41 (d, J=8.7 Hz, 1H), 7.19-6.97 (m, 2H), 4.86 (tt, J=7.1, 3.8 Hz,1H), 3.84 (dq, J=6.6, 4.7 Hz, 1H), 3.21 (s, 3H), 2.40 (dt, J=14.1, 7.0Hz, 1H), 2.02 (dtd, J=15.1, 7.6, 5.8 Hz, 1H), 1.89-1.74 (m, 3H), 1.70(dt, J=14.4, 4.0 Hz, 1H).

6-fluoro-3-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A357”)

UPLC/MS 0.77 min, [M+H]⁺ 337;

¹H NMR (400 MHz, DMSO-d₆) δ 12.25 (s, 1H), 9.11 (s, 1H), 8.82 (s, 1H),8.09-7.86 (m, 2H), 7.79 (dd, J=9.1, 2.5 Hz, 1H), 7.58-7.36 (m, 2H),7.23-7.01 (m, 2H), 3.86 (s, 3H).

6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A358”)

HPLC/MS 1.63 min (A), [M+H]⁺ 470;

¹H NMR (700 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.40 (s, 1H), 8.88 (s, 1H),8.31 (d, J=8.7 Hz, 2H), 8.13-7.97 (m, 2H), 7.82 (dd, J=9.1, 2.8 Hz, 1H),7.47 (td, J=8.8, 2.9 Hz, 1H), 7.43 (dd, J=9.0, 4.8 Hz, 1H), 3.86 (dq,J=5.7, 3.0 Hz, 1H), 3.37-3.30 (m, 3H), 3.17 (td, J=9.6, 7.2 Hz, 1H),3.04 (s, 3H), 1.92-1.72 (m, 2H).

6-chloro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A359”)

HPLC/MS 1.73 min (A), [M+H]⁺ 486;

¹H NMR (400 MHz, DMSO-d₆) δ 12.35 (s, 1H), 9.38 (s, 1H), 8.86 (s, 1H),8.38-8.23 (m, 2H), 8.06 (d, J=2.3 Hz, 1H), 8.05-7.97 (m, 2H), 7.60 (dd,J=8.8, 2.3 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 3.87 (p, J=3.2 Hz, 1H),3.38-3.30 (m, 3H), 3.18 (td, J=9.4, 7.5 Hz, 1H), 1.89-1.70 (m, 2H).

6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A360”)

HPLC/MS 1.63 min (A), [M+H]⁺ 470;

¹H NMR (700 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.40 (s, 1H), 8.88 (s, 1H),8.31 (d, J=8.7 Hz, 2H), 8.13-7.97 (m, 2H), 7.82 (dd, J=9.1, 2.8 Hz, 1H),7.47 (td, J=8.8, 2.9 Hz, 1H), 7.43 (dd, J=9.0, 4.8 Hz, 1H), 3.86 (dq,J=5.7, 3.0 Hz, 1H), 3.37-3.30 (m, 3H), 3.17 (td, J=9.6, 7.2 Hz, 1H),3.04 (s, 3H), 1.92-1.72 (m, 2H).

6-chloro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A361”)

HPLC/MS 1.73 min (A), [M+H]+ 486;

¹H NMR (400 MHz, DMSO-d₆) δ 12.35 (s, 1H), 9.38 (s, 1H), 8.86 (s, 1H),8.38-8.23 (m, 2H), 8.06 (d, J=2.3 Hz, 1H), 8.05-7.97 (m, 2H), 7.60 (dd,J=8.8, 2.3 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 3.87 (p, J=3.2 Hz, 1H),3.38-3.30 (m, 3H), 3.18 (td, J=9.4, 7.5 Hz, 1H), 1.89-1.70 (m, 2H).

6-fluoro-3-{1-[4-((1S,2S)-2-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A362”)

HPLC/MS 1.83 min (A), [M+H]⁺ 421;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.13 (s, 1H), 8.84 (s, 1H),8.03-7.86 (m, 2H), 7.81 (dd, J=9.2, 2.8 Hz, 1H), 7.46 (td, J=8.8, 2.8Hz, 1H), 7.42 (dd, J=9.0, 4.9 Hz, 1H), 7.20-7.13 (m, 2H), 4.74 (dt,J=6.0, 2.9 Hz, 1H), 3.85 -3.81 (m, 1H), 3.30 (s, 3H), 2.19-2.07 (m, 1H),2.03-1.90 (m, 1H), 1.75-1.61 (m, 4H).

6-chloro-3-[1-(4-cyclopentyloxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A363”)

UPLC/MS 0.97 min, [M+H]⁺ 407;

¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.11 (s, 1H), 8.82 (s, 1H),8.06 (d, J=2.4 Hz, 1H), 7.95-7.82 (m, 2H), 7.59 (dd, J=8.8, 2.4 Hz, 1H),7.40 (d, J=8.8 Hz, 1H), 7.16-7.06 (m, 2H), 4.95-4.90 (m, 1H), 2.07-1.85(m, 2H), 1.84-1.68 (m, 4H), 1.67-1.57 (m, 2H).

3-[1-(4-cyclopentyloxy-phenyl)-1H-[1,2,3]triazol-4-yl]-6-fluoro-1H-quinolin-2-one(“A364”)

UPLC/MS 0.91 min, [M+H]⁺ 391;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.11 (s, 1H), 8.83 (s, 1H),7.91-7.85 (m, 2H), 7.81 (dd, J=9.3, 2.8 Hz, 1H), 7.46 (td, J=8.8, 2.8Hz, 1H), 7.42 (dd, J=9.1, 4.9 Hz, 1H), 7.15-7.09 (m, 2H), 4.95-4.90 (m,1H), 2.02-1.92 (m, 2H), 1.80-1.68 (m, 4H), 1.68-1.56 (m, 2H).

6-fluoro-3-{1-[4-(tetrahydro-furan-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A365”)

UPLC/MS 0.77 min, [M+H]⁺ 393;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.13 (s, 1H), 8.83 (s, 1H),8.04-7.87 (m, 2H), 7.81 (dd, J=9.2, 2.8 Hz, 1H), 7.46 (td, J=8.8, 2.8Hz, 1H), 7.42 (dd, J=9.0, 4.9 Hz, 1H), 7.18-7.11 (m, 2H), 5.15 (ddt,J=6.2, 3.9, 1.7 Hz, 1H), 3.93 (dd, J=10.2, 4.5 Hz, 1H), 3.91-3.82 (m,2H), 3.79 (td, J=8.4, 4.6 Hz, 1H), 2.28 (dtd, J=16.4, 8.2, 6.2 Hz, 1H),2.06-1.94 (m, 1H).

6-chloro-3-{1-[4-(tetrahydro-furan-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A366”)

UPLC/MS 0.82 min, [M+H]⁺ 409;

¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.12 (s, 1H), 8.82 (s, 1H),8.06 (d, J=2.3 Hz, 1H), 7.98-7.83 (m, 2H), 7.59 (dd, J=8.8, 2.4 Hz, 1H),7.40 (d, J=8.8 Hz, 1H), 7.14 (d, J=9.0 Hz, 2H), 5.14 (ddd, J=6.2, 4.2,1.9 Hz, 1H), 3.93 (dd, J=10.2, 4.5 Hz, 1H), 3.91-3.82 (m, 2H), 3.79 (td,J=8.4, 4.6 Hz, 1H), 2.28 (dtd, J=14.4, 8.2, 6.2 Hz, 1H), 2.07-1.95 (m,1H).

Example 107-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A117”) and7-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A118”)

To a suspension of4-[4-(4-carboxymethyl-[1,2,3]triazol-1-yl)-benzoyl]-piperazine-1-carboxylicacid tert-butyl ester (291 mg, 0.70 mmol) and2-Amino-4-fluoro-benzaldehyde (97.4 mg, 0.7 mmol) in acetic acidanhydride (1.17 ml) is added triethylamine (388 μl, 2.80 mmol) and thereaction mixture is stirred for 16 hours at room temperature. Thereaction mixture is treated with dichloromethane and water. The organicphase is separated and the aqueous phase is extracted withdichloromethane. The combined organic phases are dried over sodiumsulfate and evaporated. The residue is chromatographed on a silica gelcolumn with dichloromethane/methanol as eluent to afford4-{4-[4-(7-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperazine-1-carboxylicacid tert-butyl ester as beige solid; HPLC/MS 1.70 min (A), [M+H]+ 519.

Example 10A Synthesis of “A117”

A suspension of4-{4-[4-(7-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperazine-1-carboxylicacid tert-butyl ester (83.0 mg, 0.16 mmol) in a 4 M solution ofhydrochloric acid in dioxane (362 μl) is heated to 70° C. and stirred atthis temperature in a closed reaction vial for 4 hours. The reactionmixture is allowed to reach room temperature and concentrated undervacuum. The residue is treated with saturated Na₂CO₃ solution and themixture is evaporated. The solid residue is extracted with a mixture ofdichloromethane and methanol. The extraction solution is evaporated andthe residue is chromatographed on a silica gel column withdichloromethane/methanol as eluent to afford7-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas off-white solid; HPLC/MS 1.18 min (A), [M+H]+ 419. ¹H NMR (400 MHz,DMSO-d₆, TFA-d₁) δ 9.26 (s, 1H), 8.87 (s, 1H), 8.11 (d, J=8.6 Hz, 2H),7.90 (dd, J=8.8, 6.0 Hz, 1H), 7.74 (d, J=8.6 Hz, 2H), 7.22 (dd, J=10.2,2.5 Hz, 1H), 7.06 (td, J=8.8, 2.5 Hz, 1H), 3.83 (bs, 4H), 3.27 (bs, 4H).

The following compounds are prepared similarly:

5-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A119”)

beige solid; HPLC/MS 1.20 min (A), [M+H]+ 419; ¹H NMR (400 MHz, DMSO-d₆,TFA-d₁) δ 9.17 (s, 1H), 8.84 (s, 1H), 8.00 (d, J=8.7 Hz, 2H), 7.62 (d,J=8.6 Hz, 2H), 7.40 (td, J=8.2, 5.9 Hz, 1H), 7.19 (d, J=8.3 Hz, 1H),6.95-6.86 (m, 1H), 3.72 (bs, 4H), 3.15 (bs, 4H).

8-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A120”)

beige solid; HPLC/MS 1.17 min (A), [M+H]⁺ 419; ¹H NMR (500 MHz, DMSO-d₆,TFA-d₁) δ 9.27 (s, 1H), 8.90 (d, J=1.5 Hz, 1H), 8.09 (d, J=8.6 Hz, 2H),7.73 (d, J=8.5 Hz, 2H), 7.66 (d, J=7.8 Hz, 1H), 7.37 (ddd, J=11.0, 8.1,1.2 Hz, 1H), 7.23 (td, J=8.0, 4.8 Hz, 1H), 3.85 (bs, 4H), 3.27 (bs, 4H).

3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A121”)

beige solid; HPLC/MS 1.05 min (A), [M+H]+ 402; ¹H NMR (400 MHz, DMSO-d₆,TFA-d₁) δ 9.21 (s, 1H), 8.83 (s, 1H), 8.52 (dd, J=4.9, 1.8 Hz, 1H), 8.31(dd, J=7.9, 1.7 Hz, 1H), 8.04 (d, J=8.6 Hz, 2H), 7.66 (d, J=8.6 Hz, 2H),7.27 (dd, J=7.8, 4.9 Hz, 1H), 3.72 (bs, 4H), 3.18 (bs, 4H).

6-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A122”)

beige solid; HPLC/MS 1.08 min (A), [M+H]⁺ 420; ¹H NMR (400 MHz, DMSO-d₆)δ 12.74 (s, 1H), 9.32 (s, 1H), 9.30 (bs, 1H), 8.88 (s, 1H), 8.63 (d,J=2.7 Hz, 1H), 8.37 (dd, J=8.7, 2.9 Hz, 1H), 8.13 (d, J=8.6 Hz, 2H),7.73 (d, J=8.6 Hz, 2H), 3.75 (bs, 4H), 3.19 (s, 4H).

6-chloro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A123”)

off-white solid; HPLC/MS 1.26 min (A), [M+H]⁺ 435; ¹H NMR (400 MHz,DMSO-d₆) δ 12.35 (s, 1H), 9.30 (s, 1H), 9.28 (bs, 1H), 8.85 (s, 1H),8.13 (d, J=8.5 Hz, 2H), 8.06 (d, J=2.3 Hz, 1H), 7.73 (d, J=8.6 Hz, 1H),7.60 (dd, J=8.7, 2.4 Hz, 1H), 7.43 (d, J=8.7 Hz, 1H), 3.75 (bs, 4H),3.20 (s, 4H).

3-[1-(4-[1,4]diazepan-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-6-fluoro-1H-[1,8]naphthyridin-2-one(“A124”)

green-brown solid; HPLC/MS 1.17 min (A), [M+H]⁺ 406; ¹H NMR (400 MHz,DMSO-d₆, TFA-d₁) δ 9.05 (s, 1H), 8.84 (s, 1H), 8.52 (d, J=2.9 Hz, 1H),8.18 (dd, J=8.5, 2.9 Hz, 1H), 7.78 (d, J=9.1 Hz, 2H), 6.99 (d, J=9.2 Hz,2H), 3.85 (t, J=5.2 Hz, 2H), 3.65 (t, J=6.1 Hz, 2H), 3.38 (t, J=5.1 Hz,2H), 3.29-3.19 (m, 2H), 2.19 (p, J=5.9 Hz, 2H).

6-fluoro-3-{1-[3-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A125”)

beige solid; HPLC/MS 1.19 min (A), [M+H]+ 419; ¹H NMR (400 MHz, DMSO-d₆,TFA-d₁) δ 9.31 (s, 1H), 8.86 (s, 1H), 8.18-8.10 (m, 2H), 7.75-7.64 (m,2H), 7.59 (d, J=7.6 Hz, 1H), 7.50 (dd, J=9.0, 4.7 Hz, 1H), 7.37 (td,J=8.8, 2.8 Hz, 1H), 3.89 (bs, 4H), 3.27 (s, 4H).

7-chloro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A126”)

white solid; HPLC/MS 1.27 min (A), [M+H]⁺ 435; ¹H NMR (400 MHz, DMSO-d₆)δ 12.28 (bs, 1H), 9.25 (s, 1H), 8.85 (s, 1H), 8.08 (d, J=8.6 Hz, 2H),7.95 (d, J=8.5 Hz, 1H), 7.62 (d, J=8.6 Hz, 2H), 7.42 (d, J=2.0 Hz, 1H),7.30 (dd, J=8.4, 2.0 Hz, 1H), 3.65-3.35 (m, 4H), 2.72 (bs, 4H).

5,6-difluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A127”)

beige solid; HPLC/MS 1.20 min (A), [M+H]+ 437; ¹H NMR (400 MHz, DMSO-d₆,TFA-d₁) δ 9.27 (s, 1H), 8.83 (s, 1H), 8.13-8.04 (m, 2H), 7.69 (d, J=8.2Hz, 2H), 7.51 (q, J=9.3, 8.9 Hz, 1H), 7.22 (dd, J=9.4, 3.6 Hz, 1H), 3.73(bs, 4H), 3.20 (bs, 4H).

6,7-difluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A128”)

hydrochloride: beige solid; UPLC/MS 0.48 min, [M+H]⁺ 437; ¹H NMR (500MHz, DMSO-d6) δ 12.35 (s, 1H), 9.29 (s, 1H), 8.97 (bs, 2H), 8.85 (s,1H), 8.23-8.02 (m, 3H), 7.71 (d, J=8.5 Hz, 2H), 7.35 (dd, J=11.4, 7.0Hz, 1H), 3.71 (bs, 4H), 3.16 (bs, 4H).

6-fluoro-3-{1-[4-(piperazine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A129”)

hydrochloride: beige powder; UPLC/MS 0.50 min, [M+H]⁺ 455; ¹H NMR (500MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.42 (s, 1H), 9.07 (s, 2H), 8.87 (s, 1H),8.58-8.28 (m, 2H), 8.17-7.95 (m, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H),7.56-7.37 (m, 2H), 3.26-3.19 (m, 8H).

6,7-difluoro-3-{1-[4-(2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A130”)

light brown solid; HPLC/MS 1.20 min (A), [M+H]⁺ 453.

6-fluoro-3-{1-[4-(3-piperazin-1-yl-propoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A131”)

off-white powder; HPLC/MS 1.15 min (A), [M+H]⁺ 449.

6-fluoro-3-{1-[4-(piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A132”)

hydrochloride: beige solid; HPLC/MS 1.25 min (A), [M+H]⁺ 418. ¹H NMR(500 MHz, DMSO-d₆) δ 12.31 (s, 1H), 9.40 (s, 1H), 8.88 (s, 1H), 8.64 (d,J=11.5 Hz, 1H), 8.45-8.33 (m, 1H), 8.25 (m, 4H), 7.83 (dd, J=9.2, 2.7Hz, 1H), 7.48 (td, J=8.7, 2.8 Hz, 1H), 7.44 (dd, J=9.1, 5.0 Hz, 1H),3.86 (tt, J=11.2, 3.6 Hz, 1H), 3.37 (d, J=13.0 Hz, 2H), 3.15-3.02 (m,2H), 2.06-1.96 (m, 2H), 1.79 (dtd, J=14.5, 11.4, 10.9, 4.0 Hz, 2H).

6-fluoro-3-{1-[4-(2-piperidin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A133”)

beige solid; HPLC/MS 1.31 min (A), [M+H]+ 434.

6,7-difluoro-3-{1-[4-(2-piperidin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A134”)

off-white solid; HPLC/MS 1.34 min (A), [M+H]⁺ 452.

6,7-difluoro-3-{1-[4-(3-piperazin-1-yl-propoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A135”)

off-white powder; HPLC/MS 1.19 min (A), [M+H]⁺ 467.

6,7-difluoro-3-{1-[4-(piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A136”)

hydrochloride; beige solid; UPLC/MS 0.76 min, [M+H]⁺ 436. ¹H NMR (400MHz, DMSO-d₆) δ 12.36 (s, 1H), 9.37 (s, 1H), 8.86 (s, 1H), 8.83 (bs,1H), 8.55 (bs, 1H), 8.24 (s, 4H), 8.10 (dd, J=11.0, 8.6 Hz, 1H), 7.35(dd, J=11.5, 7.1 Hz, 1H), 3.86 (ddd, J=11.2, 7.7, 3.5 Hz, 1H), 3.33 (m,2H), 3.08 (q, J=11.8 Hz, 2H), 2.01 (d, J=14.0 Hz, 2H), 1.89-1.68 (m,2H).

6-methyl-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A137”)

hydrochloride: beige solid; UPLC/MS 0.72 min, [M+H]⁺ 415. ¹H NMR (500MHz, DMSO-d₆) δ 12.14 (s, 1H), 9.28 (s, 1H), 9.14 (bs, 2H), 8.77 (s,1H), 8.29-8.00 (m, 2H), 7.75-7.70 (m, 2H), 7.69 (bs, 1H), 7.41 (dd,J=8.4, 1.9 Hz, 1H), 7.33 (d, J=8.3 Hz, 1H), 3.74 (bs, 4H), 3.20 (bs,4H), 2.40 (s, 3H).

5,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A138”)

hydrochloride: beige solid; UPLC/MS 0.92 min, [M+H]⁺ 490. ¹H NMR (400MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.29 (bs, 2H), 9.11 (s, 1H), 8.84 (s,1H), 8.12 (d, J=2.1 Hz, 1H), 8.09 (dd, J=11.1, 8.7 Hz, 1H), 7.69 (dd,J=8.8, 2.1 Hz, 1H), 7.62 (d, J=8.9 Hz, 1H), 7.41 (d, J=3.1 Hz, 1H), 7.35(dd, J=11.5, 7.1 Hz, 1H), 5.34 (s, 2H), 3.84 (bs, 2H), 3.71 (bs, 2H),3.26 (bs, 2H), 3.12 (bs, 2H).

6,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A139”)

hydrochloride: light yellow solid; UPLC/MS 0.93 min, [M+H]⁺ 490.

6,7-difluoro-3-{1-[4-(2-oxo-2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A140”)

hydrochloride: beige solid; UPLC/MS 0.87 min, [M+H]+ 467. ¹H NMR (400MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.15 (bs, 2H), 9.10 (s, 1H), 8.82 (s,1H), 8.08 (dd, J=11.0, 8.6 Hz, 1H), 7.93-7.83 (m, 2H), 7.34 (dd, J=11.5,7.1 Hz, 1H), 7.24-7.11 (m, 2H), 5.01 (s, 2H), 3.71 (bs, 4H), 3.20 (bs,2H), 3.11 (bs, 2H).

6-fluoro-3-{1-[4-(2-oxo-2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A141”)

hydrochloride: beige solid; UPLC/MS 0.84 min, [M+H]⁺ 449.

3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-trifluoromethyl-1H-quinolin-2-one(“A142”)

hydrochloride: beige solid; UPLC/MS 0.92 min, [M+H]⁺ 469.

3-{1-[4-(4-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A143”)

hydrochloride: light beige solid; UPLC/MS 0.85 min, [M+H]⁺ 451.

3-{1-[4-(4-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A144”)

hydrochloride: beige solid; UPLC/MS 0.81 min, [M+H]⁺ 433.

6,7-difluoro-3-{1-[4-(2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A145”)

hydrochloride: light brown solid; HPLC/MS 1.20 min (A), [M+H]⁺ 423. ¹HNMR (400 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.72 (s, 2H), 9.23 (s, 1H), 8.84(s, 1H), 8.13-8.03 (m, 3H), 7.64-7.55 (m, 2H), 7.34 (dd, J=11.5, 7.1 Hz,1H), 3.96 (bs, 2H), 3.91 (s, 2H), 3.57 (bs, 2H).

6,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indazol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A146”)

trifluoroacetate: brown solid; UPLC/MS 0.48 min, [M+H]⁺ 491. ¹H NMR (400MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.21 (s, 1H), 8.85 (s, 1H), 8.76 (s, 2H),8.39 (d, J=2.0 Hz, 1H), 8.24 (d, J=0.9 Hz, 1H), 8.09 (dd, J=11.0, 8.6Hz, 1H), 8.02 (dd, J=9.0, 2.1 Hz, 1H), 7.80 (d, J=9.0 Hz, 1H), 7.33 (dd,J=11.4, 7.1 Hz, 1H), 5.61 (s, 2H), 3.80 (bs, 2H), 3.65 (bs, 2H), 3.26(bs, 2H), 3.12 (bs, 2H).

6-fluoro-7-methoxy-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A147”)

light beige solid; HPLC/MS 1.20 min (A), [M+H]⁺ 449. ¹H NMR (400 MHz,DMSO-d₆) δ 12.18 (s, 1H), 9.24 (s, 1H), 9.09 (s, 2H), 8.77 (s, 1H), 8.12(d, J=8.6 Hz, 2H), 7.83 (d, J=11.6 Hz, 1H), 7.77-7.66 (m, 2H), 7.08 (d,J=7.6 Hz, 1H), 3.93 (s, 3H), 3.74 (bs, 4H), 3.20 (b, 4H).

6-chloro-7-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A148”)

hydrochloride: beige solid; UPLC/MS 0.49 min, [M+H]⁺ 453. ¹H NMR (400MHz, DMSO-d₆) δ 12.41 (s, 1H), 9.28 (s, 1H), 9.21 (bs, 2H), 8.85 (s,1H), 8.27 (d, J=8.0 Hz, 1H), 8.13 (d, J=8.6 Hz, 2H), 7.72 (d, J=8.6 Hz,2H), 7.33 (d, J=10.3 Hz, 1H), 3.36 (bs, 4H), 3.19 (bs, 4H).

Example 10b Synthesis of “A118”

To a solution of4-{4-[4-(7-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperazine-1-carboxylicacid tert-butyl ester (83.0 mg, 0.16 mmol) in formic acid (0.9 ml) isadded formaldehyde (37% aqueous solution, 36.5 μl, 0.49 mmol) and thereaction mixture is stirred for 2 hours at 80° C. The reaction mixtureis concentrated under reduced pressure and treated with saturated NaHCO₃solution. The resultant precipitate is filtered off, washed with waterand dried under vacuum. The residue is chromatographed on a silica gelcolumn with dichloromethane/methanol as eluent to afford7-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A118”) as off-white solid; HPLC/MS 1.19 min (A), [M+H]⁺ 433.

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.23 (s, 1H), 8.85 (s, 1H),8.08 (d, J=8.6 Hz, 2H), 7.99 (dd, J=9.5, 6.1 Hz, 1H), 7.62 (d, J=8.6 Hz,2H), 7.18 -7.09 (m, 2H), 3.86-3.32 (m, 4H), 2.35 (bs, 4H), 2.21 (s, 3H).

The following compounds are prepared similarly:

5-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A149”)

beige solid; HPLC/MS 1.22 min (A), [M+H]+ 433; ¹H NMR (400 MHz, DMSO-d₆)δ 12.46 (s, 1H), 9.30 (s, 1H), 8.83 (s, 1H), 8.10 (d, J=8.6 Hz, 2H),7.64 (d, J=8.5 Hz, 2H), 7.58 (td, J=8.2, 6.0 Hz, 1H), 7.26 (d, J=8.3 Hz,1H), 7.17-7.08 (m, 1H), 3.75-3.30 (m, 4H), 2.35 (bs, 4H), 2.23 (s, 3H).

8-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A150”)

off-white solid; HPLC/MS 1.17 min (A), [M+H]+ 433; ¹H NMR (500 MHz,DMSO-d₆) (12.24 (s, 1H), 9.28 (s, 1H), 8.88 (d, J=1.5 Hz, 1H), 8.13-8.05(m, 2H), 7.75 (dd, J=8.0, 1.1 Hz, 1H), 7.66-7.59 (m, 2H), 7.46 (ddd,J=11.1, 8.1, 1.2 Hz, 1H), 7.24 (td, J=8.0, 4.9 Hz, 1H), 3.78-3.30 (m,4H), 2.44-2.27 (m, 4H), 2.21 (s, 3H).

6-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A151”)

off-white solid; HPLC/MS 1.31 min (A), [M+H]+ 449; ¹H NMR (400 MHz,DMSO-d₆) δ 12.32 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.10 (d, J=8.5 Hz,2H), 8.07 (d, J=2.4 Hz, 1H), 7.63 (d, J=8.5 Hz, 2H), 7.60 (dd, J=9.1,2.7 Hz, 1H), 7.42 (d, J=8.8 Hz, 1H), 3.75-3.30 (m, 4H), 2.36 (bs, 4H),2.23 (s, 3H).

5,7-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A152”)

beige solid; HPLC/MS 1.25 min (A), [M+H]⁺ 451; ¹H NMR (500 MHz, DMSO-d₆)δ 12.54 (s, 1H), 9.28 (s, 1H), 8.77 (s, 1H), 8.10 (d, J=8.6 Hz, 2H),7.63 (d, J=8.6 Hz, 2H), 7.24 (td, J=10.0, 2.4 Hz, 1H), 7.03 (dt, J=9.8,1.7 Hz, 1H), 3.72-3.32 (m, 4H), 2.35 (bs, 4H), 2.22 (s, 3H).

6-Fluoro-3-{1-[3-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A153”)

off-white solid; HPLC/MS 1.20 min (A), [M+H]+ 433; ¹H NMR (400 MHz,DMSO-d₆) δ 12.27 (s, 1H), 9.30 (s, 1H), 8.84 (s, 1H), 8.10 (ddd, J=8.1,2.3, 1.0 Hz, 1H), 8.02 (t, J=1.8 Hz, 1H), 7.80 (dd, J=9.2, 2.6 Hz, 1H),7.68 (t, J=7.9 Hz, 1H), 7.50 (dt, J=7.6, 1.3 Hz, 1H), 7.49-7.39 (m, 2H),3.75-3.30 (m, 4H), 2.45 -2.25 (m, 4H), 2.21 (s, 3H).

7-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A154”)

white solid; HPLC/MS 1.27 min (A), [M+H]⁺ 449; ¹H NMR (400 MHz, DMSO-d₆)δ 12.28 (s, 1H), 9.26 (s, 1H), 8.86 (s, 1H), 8.09 (d, J=8.4 Hz, 2H),7.96 (d, J=8.5 Hz, 1H), 7.62 (d, J=8.5 Hz, 2H), 7.42 (d, J=2.0 Hz, 1H),7.30 (dd, J=8.4, 2.0 Hz, 1H), 3.70-3.30 (m, 4H), 2.35 (bs, 4H), 2.22 (s,3H).

6-fluoro-3-{1-[4-(4-methyl-[1,4]diazepan-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one(“A155”)

brown solid; HPLC/MS 1.18 min (A), [M+H]⁺ 420; ¹H NMR (400 MHz, DMSO-d₆)δ 12.64 (s, 1H), 9.02 (s, 1H), 8.74 (s, 1H), 8.55 (d, J=2.9 Hz, 1H),8.22 (dd, J=8.8, 3.0 Hz, 1H), 7.68 (d, J=9.0 Hz, 2H), 6.86 (d, J=9.2 Hz,2H), 3.63-3.54 (m, 2H), 3.50 (t, J=6.2 Hz, 2H), 2.71-2.58 (m, 2H),2.49-2.45 (m, 2H), 2.27 (s, 3H), 1.92 (p, J=5.9 Hz, 3H).

5,6-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A156”)

white solid; HPLC/MS 1.21 min (A), [M+H]⁺ 451; ¹H NMR (400 MHz, DMSO-d₆)δ 12.48 (s, 1H), 9.31 (s, 1H), 8.81 (s, 1H), 8.13-8.06 (m, 2H),7.72-7.60 (m, 3H), 7.23 (ddd, J=9.3, 3.9, 1.6 Hz, 1H), 3.64 (bs, 4H),2.36 (bs, 4H), 2.23 (s, 3H).

6,7-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A157”)

white solid; UPLC/MS 0.49 min, [M+H]+ 451; ¹H NMR (500 MHz, DMSO-d₆) δ12.34 (s, 1H), 9.92 (bs, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.17-8.12 (m,2H), 8.09 (dd, J=10.9, 8.6 Hz, 1H), 7.75-7.67 (m, 2H), 7.33 (dd, J=11.4,7.1 Hz, 1H), 4.44 (bs, 2H), 3.7 (bs, 2H), 3.18 (bs, 4H), 2.81 (s, 3H).

6-fluoro-3-{1-[4-(4-methyl-piperazine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A158”)

beige powder; UPLC/MS 0.50 min, [M+H]⁺ 469; ¹H NMR (400 MHz, DMSO-d₆) δ12.31 (s, 1H), 9.39 (s, 1H), 8.87 (s, 1H), 8.51-8.15 (m, 2H), 8.14-7.90(m, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.62-7.33 (m, 2H), 2.98 (t, J=4.9Hz, 4H), 2.38 (t, J=4.9 Hz, 4H), 2.15 (s, 3H).

6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A159”)

brown solid; HPLC/MS 1.25 min (A), [M+H]⁺ 467; ¹H NMR (500 MHz, DMSO-d₆)δ 12.30 (s, 1H), 9.09 (s, 1H), 8.78 (s, 1H), 8.03 (dd, J=11.0, 8.6 Hz,1H), 7.92-7.81 (m, 2H), 7.30 (dd, J=11.5, 7.1 Hz, 1H), 7.21-7.08 (m,2H), 4.16 (t, J=5.8 Hz, 2H), 2.72 (t, J=5.8 Hz, 2H), 2.50 (m, 4H), 2.32(m, 4H), 2.15 (s, 3H).

6-fluoro-3-(1-{4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A160”)

off-white powder; HPLC/MS 1.20 min (A), [M+H]+ 463; ¹H NMR (500 MHz,DMSO-d₆) δ 12.26 (s, 1H), 9.10 (s, 1H), 8.81 (s, 1H), 7.91-7.84 (m, 2H),7.78 (dd, J=9.3, 2.6 Hz, 1H), 7.48-7.38 (m, 2H), 7.18-7.06 (m, 2H), 4.09(t, J=6.4 Hz, 2H), 2.43 (t, J=7.1 Hz, 2H), 2.42-2.26 (m, 8H), 2.15 (s,3H), 1.89 (p, J=6.7 Hz, 2H).

6-fluoro-3-{1-[4-(1-methyl-piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A161”)

light beige solid; HPLC/MS 1.24 min (A), [M+H]⁺ 432.

6,7-difluoro-3-(1-{4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A162”)

light brown powder; HPLC/MS 1.23 min (A), [M+H]⁺ 481. ¹H NMR (500 MHz,DMSO-d₆) δ 12.30 (s, 1H), 9.09 (s, 1H), 8.79 (s, 1H), 8.04 (dd, J=11.0,8.6 Hz, 1H), 7.87 (d, J=9.0 Hz, 2H), 7.30 (dd, J=11.5, 7.1 Hz, 1H), 7.13(d, J=9.0 Hz, 2H), 4.09 (t, J=6.4 Hz, 2H), 2.43 (t, J=7.1 Hz, 2H),2.45-2.24 (m, 8H), 2.15 (s, 3H), 1.89 (p, J=6.7 Hz, 2H).

6-fluoro-3-(1-{4-[2-(1-methyl-piperidin-4-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A163”)

off-white solid; HPLC/MS 1.72 min (A), [M+H]⁺ 448.

6,7-difluoro-3-{1-[4-(1-methyl-piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A164”)

formate; brown solid; UPLC/MS 0.77 min, [M+H]⁺ 450.

6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A165”)

beige solid; UPLC/MS 0.84 min, [M+H]⁺ 463.

6,7-difluoro-3-(1-{4-[2-(1-methyl-piperidin-4-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A166”)

formate: beige solid; HPLC/MS 1.35 min (A), [M+H]⁺ 466. ¹H NMR (400 MHz,DMSO-d₆) δ 12.33 (s, 1H), 9.08 (s, 1H), 8.81 (s, 1H), 8.30 (s, 1H,formate), 8.07 (dd, J=11.0, 8.6 Hz, 1H), 7.95-7.73 (m, 2H), 7.32 (dd,J=11.5, 7.1 Hz, 1H), 7.20-7.03 (m, 2H), 4.09 (t, J=6.6 Hz, 2H),2.82-2.76 (m, 2H), 2.18 (s, 3H), 1.92 (td, J=11.7, 2.6 Hz, 2H),1.65-1.72 (m, 4H), 1.50-1.40 (m, 1H), 1.25 (qd, J=12.1, 3.8 Hz, 2H).

6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A167”)

formate: beige solid; UPLC/MS 0.86 min, [M+H]⁺ 481.

6-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A168”)

off-white solid; HPLC/MS 1.22 min (A), [M+H]⁺ 429. ¹H NMR (400 MHz,DMSO-d₆) δ 12.14 (s, 1H), 9.25 (s, 1H), 8.77 (s, 1H), 8.09 (d, J=8.6 Hz,2H), 7.69 (s, 1H), 7.63 (d, J=8.6 Hz, 2H), 7.40 (dd, J=8.4, 1.9 Hz, 1H),7.32 (d, J=8.4 Hz, 1H), 3.64 (bs, 2H), 3.40 (bs, 2H), 2.39 (s, 3H), 2.36(bs, 4H), 2.22 (s, 3H).

6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A169”)

beige solid; UPLC/MS 0.97 min, [M+H]⁺ 465. ¹H NMR (400 MHz, DMSO-d₆) δ12.32 (s, 1H), 9.17 (s, 1H), 8.84 (s, 1H), 8.08 (dd, J=11.0, 8.5 Hz,1H), 8.00-7.87 (m, 2H), 7.57-7.41 (m, 2H), 7.33 (dd, J=11.4, 7.1 Hz,1H), 3.83 (s, 2H), 3.51 (dt, J=15.5, 5.0 Hz, 4H), 2.27 (t, J=5.1 Hz,4H), 2.18 (s, 3H).

3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-trifluoromethyl-1H-quinolin-2-one(“A170”)

beige solid; UPLC/MS 0.92 min, [M+H]⁺ 483. ¹H NMR (400 MHz, DMSO-d₆) δ12.48 (s, 1H), 9.32 (s, 1H), 8.95 (s, 1H), 8.17 (d, J=8.2 Hz, 1H),8.13-8.07 (m, 2H), 7.72 (s, 1H), 7.66-7.61 (m, 2H), 7.57 (dd, J=8.3, 1.7Hz, 1H), 3.73-3.34 (m, 4H), 2.34 (bs, 4H), 2.23 (s, 3H).

3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A171”)

beige solid; UPLC/MS 0.86 min, [M+H]⁺ 479.

3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A172”)

beige solid; UPLC/MS 0.83 min, [M+H]⁺ 461.

6,7-difluoro-3-(1-{1-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-1H-indazol-5-yl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A173”)

trifluoroacetate: brown solid; UPLC/MS 0.48 min, [M+H]⁺ 505. ¹H NMR (400MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.87 (s, 1H), 9.21 (s, 1H), 8.85 (s, 1H),8.39 (d, J=1.9 Hz, 1H), 8.24 (d, J=0.8 Hz, 1H), 8.09 (dd, J=11.0, 8.6Hz, 1H), 8.02 (dd, J=9.0, 2.1 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H), 7.33 (dd,J=11.4, 7.1 Hz, 1H), 5.63 (bs, 2H), 4.5-4.1 (m, 2H), 3.6-2.9 (m, 6H),2.86 (s, 3H).

6,7-difluoro-3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A174”)

beige solid; HPLC/MS 1.22 min (A), [M+H]⁺ 437. ¹H NMR (400 MHz, DMSO-d₆)δ 12.30 (s, 1H), 9.21 (s, 1H), 8.83 (s, 1H), 8.08 (dd, J=11.0, 8.6 Hz,1H), 8.05-8.00 (m, 2H), 7.62-7.55 (m, 2H), 7.33 (dd, J=11.5, 7.0 Hz,1H), 3.78-3.71 (m, 2H), 3.16 (s, 2H), 2.77 (t, J=5.4 Hz, 2H), 2.31 (s,3H).

6-fluoro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A367”)

HPLC/MS 1.23 min (A), [M+H]⁺ 406;

¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H), 9.10 (s, 1H), 8.82 (s, 1H),7.98-7.85 (m, 2H), 7.80 (dd, J=9.3, 2.6 Hz, 1H), 7.53-7.36 (m, 2H),7.17-7.02 (m, 2H), 5.05-4.93 (m, 1H), 2.81 (dd, J=10.4, 6.0 Hz, 1H),2.74-2.63 (m, 2H), 2.42-2.30 (m, 2H), 2.28 (s, 3H), 1.87-1.76 (m, 1H).

6-chloro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A368”)

HPLC/MS 1.31 min (A), [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.30 (s, 1H), 9.10 (s, 1H), 8.81 (s, 1H),8.05 (d, J=2.3 Hz, 1H), 7.87 (d, J=8.9 Hz, 2H), 7.59 (dd, J=8.8, 2.4 Hz,1H), 7.41 (d, J=8.8 Hz, 1H), 7.09 (d, J=8.9 Hz, 2H), 5.01-4.93 (m, 1H),2.81 (dd, J=10.5, 6.0 Hz, 1H), 2.76-2.63 (m, 2H), 2.43-2.29 (m, 2H),2.29 (s, 3H), 1.90-1.74 (m, 1H).

6-chloro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A369”)

HPLC/MS 1.30 min (A), [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.30 (s, 1H), 9.10 (s, 1H), 8.82 (s, 1H),8.16 (s, 1H, formate-H), 8.05 (d, J=2.4 Hz, 1H), 7.87 (d, J=9.0 Hz, 2H),7.59 (dd, J=8.8, 2.3 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 7.15-7.04 (m, 2H),5.06-4.91 (m, 1H), 2.90-2.65 (m, 3H), 2.47-2.26 (m, 5H), 1.88-1.77 (m,1H).

6-fluoro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A370”)

HPLC/MS 1.22 min (A), [M+H]⁺ 406;

¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H), 9.11 (s, 1H), 8.82 (s, 1H),8.16 (s, 1H, formate-H), 7.92-7.85 (m, 2H), 7.80 (dd, J=9.3, 2.6 Hz,1H), 7.50-7.38 (m, 2H), 7.14-7.06 (m, 2H), 5.03-4.92 (m, 1H), 2.93-2.63(m, 3H), 2.45 -2.23 (m, 5H), 1.88-1.77 (m, 1H).

6-fluoro-3-{1-[4-(1-methyl-piperidin-4-ylmethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A371”)

UPLC/MS 0.52 min, [M+H]⁺ 418;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.11 (s, 1H), 8.76 (s, 1H),7.89-7.78 (m, 2H), 7.60 (dd, J=9.1, 2.8 Hz, 1H), 7.41 (dd, J=9.0, 4.7Hz, 1H), 7.35 (d, J=8.6 Hz, 2H), 7.29 (td, J=8.8, 2.9 Hz, 1H), 3.38 (d,J=12.2 Hz, 2H), 2.90-3.74 (m, 2H), 2.70 (s, 3H), 2.61 (d, J=6.6 Hz, 2H),1.85-1.73 (m, 3H), 1.41 (q, J=12.3, 11.9 Hz, 2H).

6,7-difluoro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A372”)

UPLC/MS 0.50 min, [M+H]⁺ 424;

¹H NMR (700 MHz, DMSO-d₆) δ 12.33 (s, 1H), 10.25 (s, 1H, NH⁺), 9.13 (s,1H), 8.82 (s, 1H), 8.08 (dd, J=10.8, 8.5 Hz, 1H), 7.98-7.90 (m, 2H),7.33 (dd, J=11.3, 7.0 Hz, 1H), 7.25-7.12 (m, 2H), 5.28 (bs, 1H), 4.2-3.1(m, 4H), 2.93 (s, 3H), 2.8-2.0 (m, 2H).

6,7-difluoro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A373”)

UPLC/MS 0.50 min, [M+H]⁺ 424;

¹H NMR (700 MHz, DMSO-d₆) δ 12.33 (s, 1H), 10.25 (s, 1H, NH⁺), 9.13 (s,1H), 8.82 (s, 1H), 8.08 (dd, J=10.8, 8.5 Hz, 1H), 7.98-7.90 (m, 2H),7.33 (dd, J=11.3, 7.0 Hz, 1H), 7.25-7.12 (m, 2H), 5.28 (bs, 1H), 4.2-3.1(m, 4H), 2.93 (s, 3H), 2.8-2.0 (m, 2H).

6-chloro-3-{1-[4-(1-methyl-piperidin-4-ylmethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A374”)

UPLC/MS 0.55 min, [M+H]⁺ 434;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.18 (s, 1H), 8.83 (s, 1H),8.06 (d, J=2.4 Hz, 1H), 8.03-7.89 (m, 2H), 7.59 (dd, J=8.8, 2.4 Hz, 1H),7.47-7.39 (m, 3H), 3.44-3.26 (m, 2H), 2.96-2.81 (m, 2H), 2.74 (s, 3H),2.71-2.61 (m, 2H), 1.87-1.73 (m, 3H), 1.49-1.30 (m, 2H).

6-fluoro-3-{1-[4-(1-methyl-piperidin-4-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A375”)

HPLC/MS 1.28 min (A), [M+H]⁺ 420;

¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H), 9.10 (s, 1H), 8.82 (s, 1H),7.93-7.83 (m, 2H), 7.79 (dd, J=9.2, 2.6 Hz, 1H), 7.51-7.38 (m, 2H), 7.16(d, J=9.0 Hz, 1H), 4.48 (tt, J=8.2, 4.0 Hz, 1H), 2.67-2.58 (m, 2H),2.31-2.14 (m, 5H), 2.04-1.92 (m, 2H), 1.74-1.62 (m, 2H).

6-chloro-3-{1-[4-(1-methyl-piperidin-4-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one“A376”)

HPLC/MS 1.36 min (A), [M+H]+ 436;

¹H NMR (700 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.10 (s, 1H), 8.81 (s, 1H),8.05 (d, J=2.4 Hz, 1H), 7.91-7.74 (m, 2H), 7.58 (dd, J=8.8, 2.4 Hz, 1H),7.40 (d, J=8.7 Hz, 1H), 7.22-7.00 (m, 2H), 4.48 (tt, J=8.3, 3.9 Hz, 1H),2.71-2.58 (m, 2H), 2.22-2.17 (m, 5H), 2.00-1.94 (m, 2H), 1.71-1.64 (m,2H).

Example 116-Fluoro-3-(1-{4-[4-(2-methoxy-ethyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one(“A175”)

beige solid; HPLC/MS 1.12 min (A), [M+H]+ 478; ¹H NMR (400 MHz, DMSO-d₆)δ 12.72 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H), 8.61 (d, J=2.9 Hz, 1H),8.35 (dd, J=8.7, 3.0 Hz, 1H), 8.09 (d, J=8.5 Hz, 2H), 7.62 (d, J=8.6 Hz,2H), 3.62 (bs, 2H), 3.45 (t, J=5.7 Hz, 2H), 3.36 (bs, 2H), 3.24 (s, 3H),2.55-2.40 (m, 6H).

Example 126-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A176”)

A suspension of6-fluoro-3-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(211 mg, 0.63 mmol, prepared in analogy to example 1) in dichloromethane(6 ml) is cooled to −78° C. and boron tribromide (9.38 ml of a 1 Msolution in dichloromethane, 9.38 mmol) is added. The mixture is allowedto reach room temperature and is stirred for 18 hours. To the reactionmixture is added saturated aqueous NaHCO₃ solution. The insoluble solidthat has formed is filtered off, washed with dichloromethane and waterand dried under vacuum to afford6-fluoro-3-[1-(4-hydroxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-oneas grey solid; UPLC/MS 0.68 min, [M+H]⁺ 323.

To a suspension of6-fluoro-3-[1-(4-hydroxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(203 mg, 0.63 mmol) in THF (2 ml) are added sequentiallytriphenylphosphine (198 mg, 0.76 mmol),2-(4-methyl-piperazin-1-yl)-ethanol (109 mg, 0.76 mmol) anddiisopropylazodicarboxylate (148 μl, 0.76 mmol). The reaction mixture isstirred for 18 hours at room temperature. Triphenylphosphine (198 mg,0.76 mmol) and diisopropylazodicarboxylate (148 μl, 0.76 mmol) are addedand the reaction mixture is stirred for 55 hours at room temperature.The reaction mixture is evaporated and treated with methanol. Theinsoluble solid is collected and purified by preparative HPLC to afford6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-oneas white solid. UPLC/MS 0.49 min, [M+H]⁺ 449.

¹H NMR (400 MHz, DMSO-d₆) δ 12.25 (s, 1H), 9.11 (s, 1H), 8.82 (s, 1H),7.93-7.85 (m, 2H), 7.79 (dd, J=9.2, 2.6 Hz, 1H), 7.51-7.38 (m, 2H),7.20-7.10 (m, 2H), 4.16 (t, J=5.8 Hz, 2H), 2.72 (t, J=5.8 Hz, 2H), 2.50(bs, 4H), 2.33 (bs, 4H), 2.15 (s, 3H).

Example 133-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-2-oxo-1,2-dihydro-quinoline-7-carbonitrile(“A177”)

A reaction vial is charged with7-bromo-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(250 mg, 0.52 mmol), N-methyl-pyrrolidone (2.5 ml) and copper(I) cyanide(56.1 mg, 0.63 mmol). The reaction vial is flushed with nitrogen, closedand heated to 170°. The reaction mixture is stirred in the closedreaction vial at this temperature for 8 hours. The reaction mixture isallowed to reach room temperature and treated with water. The insolublesolids are filtered off, washed with water and dried under vacuum. Theresidue is purified by preparative HPLC to afford3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-2-oxo-1,2-dihydro-quinoline-7-carbonitrileas beige solid. HPLC/MS 1.42 min (A), [M+H]⁺ 427; ¹H NMR (400 MHz,DMSO-d₆) δ 12.48 (s, 1H), 9.34 (s, 1H), 8.94 (s, 1H), 8.18-8.08 (m, 3H),7.76-7.73 (m, 1H), 7.71-7.63 (m, 3H), 3.74-3.34 (m, 6H).

Example 146-fluoro-3-(1-{1-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-1H-indol-5-yl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A178”)

beige solid; HPLC/MS 1.23 min (A), [M+H]+ 486; ¹H NMR (400 MHz, DMSO-d₆)δ 12.25 (s, 1H), 9.13 (s, 1H), 8.85 (s, 1H), 8.12 (d, J=2.1 Hz, 1H),7.81 (dd, J=9.2, 2.4 Hz, 1H), 7.69 (dd, J=8.7, 2.1 Hz, 1H), 7.58 (d,J=8.8 Hz, 1H), 7.52-7.38 (m, 3H), 6.62 (d, J=3.2 Hz, 1H), 5.29 (bs, 2H),3.64 (bs, 2H), 3.52 (bs, 2H), 2.57 (bs, 2H), 2.45 (bs, 2H), 2.33 (s,3H).

Example 15 Acetic Acid(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidin-3-ylester (“A179”)

To a suspension of{1-[4-((R)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid (94.9 mg, 0.30 mmol) and 2-amino-5-fluoro-benzaldehyde (41.7 mg,0.3 mmol) in acetic acid anhydride (1 ml) is added triethylamine (166μl, 1.2 mmol) and the reaction mixture is stirred for 30 minutes at 80°C. The reaction mixture is allowed to reach room temperature andconcentrated under vacuum. The residue is chromatographed on a silicagel column with dichloromethane/methanol as eluent to afford acetic acid(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidin-3-ylester as off-white solid; HPLC/MS 1.49 min (A), [M+H]⁺ 462. ¹H NMR (400MHz, DMSO-d₆): 1:1 mixture of rotamers, selection of peaks: δ 12.27 (s,1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.09 (d, J=8.4 Hz, 2H), 7.86-7.73 (m,3H), 7.51-7.39 (m, 2H), 2.06 (s, rotamer1), 1.99 (s, rotamer2).

Acetic Acid(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidin-3-ylester (“A180”)

is prepared similarly: off-white solid; HPLC/MS 1.49 min (A), [M+H]⁺462. ¹H NMR (400 MHz, DMSO-d₆): 1:1 mixture of rotamers, selection ofpeaks: δ 12.27 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.09 (d, J=8.4 Hz,2H), 7.86-7.73 (m, 3H), 7.51-7.39 (m, 2H), 2.06 (s, rotamer1), 1.99 (s,rotamer2).

Example 166-fluoro-3-{1-[4-((R)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A181”)

To a solution of acetic acid(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidin-3-ylester (94.9 mg, 0.30 mmol) and 2-amino-5-fluorobenzaldehyde (21.9 mg,0.05 mmol) in methanol (1 ml) is added 1 M sodium hydroxide solution (1ml) and the reaction mixture is stirred for 3 hours at room temperature.The reaction mixture is concentrated under vacuum and the residue istreated with water. The resultant precipitate is filtered off, washedwith water and dried under vacuum to afford6-fluoro-3-{1-[4-((R)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas off-white solid; HPLC/MS 1.34 min (A), [M+H]⁺ 420.

¹H NMR (400 MHz, DMSO-d₆): 1:1 mixture of rotamers, selection of peaks:δ 12.26 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H), 8.15-8.03 (m, 2H), 7.80(dd, J=9.2, 2.6 Hz, 1H), 7.75 (m, 2H), 7.52-7.37 (m, 2H), 5.02 (d, J=3Hz, rotamer1), 4.96 (d, J=3.1 Hz, rotamer2), 4.35 (bs, rotamer1), 4.27(bs, rotamer2).

The following compounds are prepared similarly:

6-fluoro-3-{1-[4-((S)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A182”)

off-white solid; HPLC/MS 1.34 min (A), [M+H]⁺ 420; ¹H NMR (400 MHz,DMSO-d₆): 1:1 mixture of rotamers, selection of peaks: δ 12.26 (s, 1H),9.29 (s, 1H), 8.85 (s, 1H), 8.15-8.03 (m, 2H), 7.80 (dd, J=9.2, 2.6 Hz,1H), 7.75 (m, 2H), 7.52-7.37 (m, 2H), 5.02 (d, J=3 Hz, rotamer1), 4.96(d, J=3.1 Hz, rotamer2), 4.35 (bs, rotamer1), 4.27 (bs, rotamer2).

6-fluoro-3-{1-[4-(4-hydroxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A183”)

off-white solid; HPLC/MS 1.36 min (A), [M+H]⁺ 434; ¹H NMR (500 MHz,DMSO-d₆) δ 12.34 (s, 1H), 9.34 (s, 1H), 8.91 (s, 1H), 8.21-8.00 (m, 2H),7.86 (dd, J=9.3, 2.8 Hz, 1H), 7.74-7.60 (m, 2H), 7.59-7.39 (m, 2H), 4.85(d, J=3.9 Hz, 1H), 4.08 (bs, 1H), 3.83 (tq, J=8.0, 3.8 Hz, 1H), 3.59(bs, 1H), 3.29 (bs, 2H), 1.84 (m, 2H), 1.46 (m, 2H).

6-fluoro-3-{1-[4-(3-hydroxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A184”)

beige solid; HPLC/MS 1.40 min (A), [M+H]⁺ 434.

Example 174-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A185”)

To a suspension of{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-aceticacid (94.9 mg, 0.30 mmol) and 1-(2-amino-phenyl)-ethanone (40.6 mg, 0.3mmol) in acetic acid anhydride (1 ml) is added triethylamine (166 μl,1.2 mmol) and the reaction mixture is stirred for 5 hours at 100° C. Thereaction mixture is allowed to reach room temperature and water isadded. The solids are filtered off and partially dissolved in a smallamount of DMSO. Methanol is added. The solid is filtered off, washedwith methanol and dried under vacuum to afford4-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas brown powder; UPLC/MS 0.87 min, [M+H]⁺ 416.

¹H NMR (400 MHz, DMSO-d₆) δ 11.98 (s, 1H), 9.10 (s, 1H), 8.20-8.03 (m,2H), 7.91 (dd, J=8.3, 1.3 Hz, 1H), 7.76-7.63 (m, 2H), 7.57 (ddd, J=8.3,7.1, 1.3 Hz, 1H), 7.38 (dd, J=8.2, 1.2 Hz, 1H), 7.27 (ddd, J=8.3, 7.1,1.2 Hz, 1H), 3.70 -3.35 (m, 8H), 2.65 (s, 3H).

Example 186-fluoro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A186”)

To a suspension of copper(II) sulfate pentahydrate (449 mg, 1.80 mmol)and sodium(2R)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxy-ethanolatehydrate (389 mg, 1.80 mmol) in a mixture of tert-butanol (20 ml) andwater (20 ml) are added 3-butynoic acid (1.51 g, 18.0 mmol) and4-azido-benzoic acid methyl ester (3.19 g, 18.0 mmol). The reactionmixture is stirred at 80° C. for 3 hours. The reaction mixture isallowed to reach room temperature and poured into water. The resultantprecipitate is filtered off, washed with water and dried under vacuum toafford 4-(4-carboxymethyl-[1,2,3]triazol-1-yl)-benzoic acid methyl esteras beige solid; UPLC/MS 0.55 min, [M+H]⁺ 262.

To a suspension of 4-(4-carboxymethyl-[1,2,3]triazol-1-yl)-benzoic acidmethyl ester (1.23 g, 4.70 mmol) and 2-amino-5-fluoro-benzaldehyde (654mg, 4.70 mmol) in acetic acid anhydride (4 ml) is added triethylamine(2.61 ml, 18.8 mmol) and the reaction mixture is stirred for 30 minutesat 80° C. The reaction mixture is diluted cautiously with methanol. Thesolid is filtered off, washed with tert-butyl methyl ether and driedunder vacuum to afford4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid methyl ester as beige solid; UPLC/MS 0.80 min, [M+H]⁺ 365.

To a suspension of4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid methyl ester (1.24 g, 3.30 mmol) in methanol (30 ml) is addedaqueous 2 M sodium hydroxide solution (8.25 ml, 16.5 mmol) and thereaction mixture is stirred for 2 hours at 80° C. The reaction mixtureis allowed to reach room temperature and is filtered. The solid residueis triturated with excess 0.5 N hydrochloric acid. The solid is filteredoff, washed with water and acetonitrile and dried under vacuum to afford4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid as beige solid; UPLC/MS 0.70 min, [M+H]⁺ 351.

To a suspension of4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid (35.0 mg, 0.10 mmol) in a mixture of 1,4-dioxane (0.5 ml) and DMF(0.5 ml) are added (R)-2-methylpyrrolidine p-toluenesulfonate (30.9 mg,0.12 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride(28.8 mg, 0.15 mmol), 1-hydroxybenotriazole hydrate (13.5 mg, 0.10 mmol)and 4-methylmorpholine (16.5 μl, 0.15 mmol). The resultant suspension isstirred at room temperature for 5 hours. The reaction mixture is pouredinto water. The resultant precipitate is filtered off, washed with waterand dried. The residue is chromatographed on a silica gel column withdichloromethane/methanol as eluent to afford6-fluoro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-oneas white crystals; HPLC/MS 1.59 min (A), [M+H]⁺ 418.

¹H NMR (500 MHz, DMSO-d₆), mixture of rotamers; main rotamer: δ 12.31(s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.26-7.95 (m, 2H), 7.82 (dd, J=9.2,2.8 Hz, 1H), 7.73 (d, J=8.1 Hz, 2H), 7.47 (td, J=8.8, 2.8 Hz, 1H), 7.43(dd, J=9.0, 4.9 Hz, 1H), 4.25-4.14 (m, 1H), 3.57-3.51 (m, 1H), 3.37-3.32(m, 1H), 2.10 (dq, J=13.4, 6.8 Hz, 1H), 1.99-1.84 (m, 1H), 1.79-1.68 (m,1H), 1.64-1.53 (m, 1H), 1.29 (d, J=6.2 Hz, 3H).

The following compounds are prepared similarly:

N-(2-diethylamino-ethyl)-4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A187”)

HPLC/MS 1.27 min (A), [M+H]⁺ 467;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.33 (s, 1H), 8.86 (s, 1H), 8.20 (d,J=8.9 Hz, 2H), 8.15 (d, J=8.8 Hz, 2H), 7.95 (dd, J=10.8, 8.5 Hz, 1H),7.37 (dd, J=11.4, 7.0 Hz, 1H), 3.73 (t, J=6.3 Hz, 2H), 3.36 (t, J=6.3Hz, 2H), 3.30 (qd, J=7.0, 3.8 Hz, 4H), 1.29 (t, J=7.3 Hz, 6H).

4-[4-(7-chloro-6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-diethylamino-ethyl)-benzamide(“A188”)

HPLC/MS 1.36 min (A), [M+H]+ 483;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.28 (s, 1H), 8.81 (s, 1H), 8.14 (d,J=8.8 Hz, 2H), 8.08 (d, J=8.8 Hz, 2H), 7.87 (d, J=9.6 Hz, 1H), 7.52 (d,J=6.5 Hz, 1H), 3.65 (t, J=6.3 Hz, 2H), 3.29 (t, J=6.5 Hz, 2H), 3.22 (qd,J=6.9, 3.5 Hz, 3H), 1.22 (t, J=7.2 Hz, 6H).

3-(1-{4-[4-(2-diethylamino-ethyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-6,7-difluoro-1H-quinolin-2-one(“A189”)

UPLC/MS 0.48 min, [M+H]⁺ 534;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.24 (s, 1H), 8.80 (s, 1H), 8.10 (d,J=8.6 Hz, 2H), 7.90 (dd, J=10.8, 8.4 Hz, 1H), 7.69 (d, J=8.6 Hz, 2H),7.31 (dd, J=11.3, 7.1 Hz, 1H), 4,0-3,6 (m, 4H), 3.63-3.55 (m, 2H), 3.52(dt, J=10.0, 3.3 Hz, 2H), 3.5-3.35 (m, 4H), 3.20 (q, J=7.2 Hz, 4H), 1.22(t, J=7.3 Hz, 6H).

6-fluoro-3-{1-[4-(4-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A190”)

UPLC/MS 0.70 min, [M+H]+ 448;

1H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.13-8.01 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.69-7.58 (m, 2H), 7.47(dd, J=9.0, 2.7 Hz, 1H), 7.45-7.39 (m, 1H), 4,1-3,8 (m, 1H), 3.65-3.41(m, 2H), 3.27 (s, 3H), 3,4-3,1 (m, 2H), 1.87 (bs, 2H), 1.48 (bs, 2H).

6,7-difluoro-3-{1-[4-(4-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A191”)

UPLC/MS 0.73 min, [M+H]⁺ 466;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.25 (s, 1H), 8.84 (s, 1H),8.29-7.99 (m, 3H), 7.76-7.58 (m, 2H), 7.32 (dd, J=11.4, 7.1 Hz, 1H),4,1-3,8 (m, 1H), 3.65-3.41 (m, 2H), 3.27 (s, 3H), 3,4-3,1 (m, 2H), 1.87(bs, 2H), 1.48 (bs, 2H).

6,7-difluoro-3-{1-[4-((R)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A1192”)

HPLC/MS 1.56 min (A), [M+H]⁺ 466;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.13-8.04 (m, 3H), 7.61 (d, J=8.0 Hz, 2H), 7.32 (dd, J=11.4, 7.1 Hz,1H), 4.0-3-6 (m, 1H), 3.5-3.0 (m, 7H), 2.0-1.35 (m, 4H).

6,7-difluoro-3-{1-[4-((S)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A193”)

HPLC/MS 1.56 min (A), [M+H]⁺ 466;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.13-8.04 (m, 3H), 7.61 (d, J=8.0 Hz, 2H), 7.32 (dd, J=11.4, 7.1 Hz,1H), 4.0-3.6 (m, 1H), 3.5-3.0 (m, 7H), 2.0-1.35 (m, 4H).

6-fluoro-3-{1-[4-((R)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A194”)

HPLC/MS 1.52 min (A), [M+H]⁺ 448.

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.18-8.04 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.65-7.55 (m, 2H),7.52-7.37 (m, 2H), 4.0-3.6 (m, 1H), 3.5-3.0 (m, 7H), 2.01-1.34 (m, 4H).

6-fluoro-3-{1-[4-((S)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A195”)

HPLC/MS 1.52 min (A), [M+H]⁺ 448;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.18-8.04 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.65-7.55 (m, 2H),7.52-7.37 (m, 2H), 4.0-3.6 (m, 1H), 3.5-3.0 (m, 7H), 2.01-1.34 (m, 4H).

N-(2-diethylamino-ethyl)-4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A196”)

HPLC/MS 1.23 min (A), [M+H]⁺ 449;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.55 (t, J=5.7 Hz, 1H), 8.14 (d, J=8.8 Hz, 2H), 8.06 (d, J=8.8 Hz, 2H),7.81 (dd, J=9.2, 2.6 Hz, 1H), 7.56-7.36 (m, 2H), 3.38-3.32 (m, 2H),2.61-2.50 (m, 6H), 0.98 (t, J=7.1 Hz, 6H).

6-fluoro-3-{1-[4-((S)-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A197”)

MS [M+H]⁺ 434;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.29 (s, 1H), 9.30(s, 1H), 8.86 (s, 1H), 8.09 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz,1H), 7.75 (d, J=8.1 Hz, 2H), 7.51-7.39 (m, 2H), 4.88-4.68 (m, 1H), 4.18(br. s, 0,7H), 3.91 (br. s, 0,3H), 3.71-3.54 (m, 2H), 3.54-3.43 (m, 1H),3.37 (br. s, 0,7H), 3.11 (br. s, 0,3H), 2.04-1.84 (m, 3H), 1.80-1.65 (m,1H).

6-fluoro-3-{1-[4-((R)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A198”)

MS [M+H]⁺ 448:

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.09 (d, J=8.2 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.72 (d, J=8.2 Hz,2H), 7.53 -7.35 (m, 2H), 4.37-4.23 (m, 1H), 3.68-3.56 (m, 1H), 3.48 (t,J=8.5 Hz, 2H), 3.33 (s, 3H), 3.11-2.97 (m, 1H), 2.09-1.96 (m, 1H),1.96-1.82 (m, 2H), 1.81-1.68 (m, 1H).

6-fluoro-3-{1-[4-((R)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A199”)

HPLC/MS 1.51 min (A), [M+H]⁺ 448;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.11-8.05 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.70 (m, 2H),7.51-7.37 (m, 2H), 3.69-3.57 (m, 1H), 3.58-3.44 (m, 2H), 3.41-3.17 (m,6H), 2.55-2.40 (m, 1H), 2.05-1.90 (m, 1H), 1.72-1.60 (m, 1H).

6,7-difluoro-3-{1-[4-((R)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A200”)

HPLC/MS 1.55 min (A), [M+H]⁺ 466;

¹H NMR (500 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.25 (s, 1H), 8.83 (s, 1H),8.10-8-04 (m, 3H), 7.77-7.72 (m, 2H), 7.32 (dd, J=11.4, 7.0 Hz, 1H),3.69-3.57 (m, 1H), 3.58-3.44 (m, 2H), 3.42-3.46 (m, 1H), 3.36-3.19 (m,5H), 2.55-2.40 (m, 1H), 2.05-1.90 (m, 1H), 1.72-1.60 (m, 1H).

6,7-difluoro-3-{1-[4-((S)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A201”)

HPLC/MS 1.55 min (A), [M+H]⁺ 466;

¹H NMR (500 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.25 (s, 1H), 8.83 (s, 1H),8.10-8-04 (m, 3H), 7.77-7.72 (m, 2H), 7.32 (dd, J=11.4, 7.0 Hz, 1H),3.69-3.57 (m, 1H), 3.58-3.44 (m, 2H), 3.42-3.46 (m, 1H), 3.36-3.19 (m,5H), 2.55-2.40 (m, 1H), 2.05-1.90 (m, 1H), 1.72-1.60 (m, 1H).

6-fluoro-3-{1-[4-((S)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A202”)

HPLC/MS 1.51 min (A), [M+H]+ 448.

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.11-8.05 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.70 (m, 2H),7.51-7.37 (m, 2H), 3.69-3.57 (m, 1H), 3.58-3.44 (m, 2H), 3.41-3.17 (m,6H), 2.55-2.40 (m, 1H), 2.05-1.90 (m, 1H), 1.72-1.60 (m, 1H).

3-(1-{4-[3-(2-diethylamino-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-6-fluoro-1H-quinolin-2-one(“A203”)

MS [M+H]⁺ 519;

¹H NMR (400 MHz, DMSO-d₆)) mixture of 2 rotamers δ 12.27 (s, 1H), 9.29(s, 1H), 8.85 (s, 1H), 8.09 (d, J=8.3 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz,1H), 7.75 (d, J=8.6 Hz, 2H), 7.51-7.39 (m, 2H), 4.16 (s, 0,4H), 4.07 (s,0,6H), 3.64 (td, J=13.1, 12.2, 4.6 Hz, 1H), 3.53 (dt, J=23.1, 6.6 Hz,2H), 3.44-3.37 (m, 3H), 2.57 (t, J=6.2 Hz, 1H), 2.42 (q, J=7.1 Hz, 2H),2.05-1.91 (m, 2H), 0.96 (t, J=7.1 Hz, 3H), 0.88 (t, J=7.1 Hz, 3H).

6-fluoro-3-{1-[4-(2-oxa-7-aza-spiro[4.4]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A204”)

MS [M+H]⁺ 460;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.29 (d, J=3.0 Hz, 1H), 8.85(s, 1H), 8.08 (d, J=8.5 Hz, 2H), 7.84-7.72 (m, 3H), 7.51-7.38 (m, 2H),3.81 (t, J=7.1 Hz, 1H), 3.78-3.47 (m, 6H), 3.43 (s, 1H), 2.03-1.85 (m,3H), 1.82 (t, J=7.1 Hz, 1H).

6-fluoro-3-{1-[4-(2-oxa-6-aza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A205”)

MS [M+H]⁺ 446;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (d, J=4.0 Hz, 1H), 8.86(s, 1H), 8.10 (t, J=8.7 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.76 (dd,J=8.2, 6.1 Hz, 2H), 7.50-7.41 (m, 2H), 4.65 (d, J=5.9 Hz, 1H), 4.55-4.44(m, 3H), 3.74 (d, J=17.9 Hz, 2H), 3.51 (dt, J=20.1, 7.0 Hz, 2H),2.26-2.12 (m, 2H).

6-fluoro-3-{1-[4-(3-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A206”)

MS [M+H]⁺ 434;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.28 (s, 1H), 9.29(s, 1H), 8.86 (s, 1H), 8.09 (dd, J=8.6, 3.4 Hz, 2H), 7.81 (dd, J=9.2,2.7 Hz, 1H), 7.76 (d, J=8.3 Hz, 2H), 7.50-7.41 (m, 2H), 4.72 (t, J=5.3Hz, 0,4H), 4.65 (t, J=5.2 Hz, 0,6H), 3.69-3.57 (m, 1H), 3.57-3.37 (m,3H), 3.30-3.23 (m, 2H), 2.45-2.24 (m, 1H), 2.03-1.87 (m, 1H), 1.75-1.60(m, 1H).

3-{1-[4-(3-dimethylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A207”)

MS [M+H]⁺ 447;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.29 (s, 1H), 9.29(s, 1H), 8.86 (s, 1H), 8.09 (d, J=8.6 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz,1H), 7.77 (t, J=8.9 Hz, 2H), 7.50-7.40 (m, 2H), 3.81-3.72 (m, 0,5H),3.71-3.63 (m, 0,5H), 3.62-3.44 (m, 2H), 3.41-3.17 (m, 1H), 2.81-2.75 (m,0,5H), 2.74-2.64 (m, 0,5H), 2.22 (s, 3H), 2.11 (s, 3H), 2.09-2.00 (m,1H), 1.84-1.69 (m, 1H).

6-fluoro-3-(1-{4-[3-(4-hydroxy-piperidin-1-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A208”)

MS [M+H]⁺ 503;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.29 (s, 1H), 9.29(s, 1H), 8.86 (s, 1H), 8.08 (d, J=7.7 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz,1H), 7.79-7.72 (m, 2H), 7.51-7.40 (m, 2H), 3.84-3.39 (m, 5H), 3.32 (s,1H), 2.94-2.68 (m, 2H), 2.22-1.94 (m, 3H), 1.84-1.58 (m, 3H), 1.51-1.29(m, 2H).

6-fluoro-3-(1-{4-[3-(2-morpholin-4-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A209”)

UPLC/MS 0.48 min, [M+H]⁺ 533;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.13-8.08 (m, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.73 (m, 2H),7.51-7.39 (m, 2H), 4.20-4.50 (m, 1H), 3.74-3.37 (m, 12H), 2.46-2.32 (m,4H), 2.05-1.95 (m, 2H).

6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A210”)

UPLC/MS 0.69 min, [M+H]⁺ 492;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.11-8.07 (m, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.73 (m, 2H),7.49-7.40 (m, 2H), 3.73-3.14 (m, 13H), 2.54-2.42 (m, 1H), 2.08-1.90 (m,1H), 1.73-1.62 (m, 1H).

4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-methoxy-ethyl)-N-methyl-benzamide(“A211”)

HPLC/MS 1.47 min (A), [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.07 (d, J=8.1 Hz, 2H), 7.80 (dd, J=9.3, 2.6 Hz, 1H), 7.69-7.60 (m, 2H),7.50-7.39 (m, 2H), 3.72-3.55 (m, 2H), 3.45 (bs, 2H), 3.36-3.16 (m, 3H),3.00 (s, 3H).

4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-methoxy-ethyl)-N-methyl-benzamide(“A212”)

HPLC/MS 1.51 min (A), [M+H]⁺ 440;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.25 (s, 1H), 8.84 (s, 1H),8.14-8.01 (m, 3H), 7.67-7.59 (m, 2H), 7.32 (dd, J=11.4, 7.0 Hz, 1H),3.72-3.55 (m, 2H), 3.45 (bs, 2H), 3.36-3.16 (m, 3H), 3.00 (s, 3H).

6-fluoro-3-{1-[4-((R)-3-hydroxymethyl-morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A213”)

MS [M+H]⁺ 450;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.86 (s, 1H),8.09 (d, J=8.5 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.67 (d, J=8.5 Hz,2H), 7.51 -7.39 (m, 2H), 4.94 (t, J=5.5 Hz, 1H), 4.52-3.35 (m, 8H),3.30-2.94 (m, 1H).

6-fluoro-3-{1-[4-(2-hydroxymethyl-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A214”)

MS [M+H]⁺ 448;

¹H NMR (400 MHz, DMSO-d₆) δ 12.26 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.05 (d, J=8.5 Hz, 2H), 7.79 (dd, J=9.2, 2.5 Hz, 1H), 7.60 (d, J=8.5 Hz,2H), 7.51 -7.38 (m, 2H), 4.79 (t, J=5.5 Hz, 1H), 4.34 (s, 1H), 3.81-3.60(m, 2H), 3.61-3.34 (m, 1H), 3.14-2.71 (m, 1H), 1.90-1.49 (m, 6H),1.50-1.30 (m, 1H).

6-fluoro-3-{1-[4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A215”)

MS [M+H]⁺ 448;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.08 (d, J=8.7 Hz, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.71 (d, J=8.2 Hz,2H), 7.50 -7.39 (m, 2H), 4.29 (br. s, 1H), 3.61 (br. s, 1H), 3.53-3.42(m, 2H), 3.04 (br. s, 1H), 2.11-1.96 (m, 1H), 1.96-1.83 (m, 2H),1.81-1.64 (m, 1H).

6-fluoro-3-{1-[4-((S)-3-hydroxymethyl-morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A216”)

MS [M+H]⁺ 450;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.86 (s, 1H),8.09 (d, J=8.5 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.67 (d, J=8.5 Hz,2H), 7.51 -7.39 (m, 2H), 4.94 (t, J=5.5 Hz, 1H), 4.52-3.35 (m, 8H),3.30-2.94 (m, 1H).

3-{1-[4-((2S,5S)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A217”)

UPLC/MS 0.75 min, [M+H]⁺ 492;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.27-8.03 (m, 2H), 7.82 (dd, J=9.2, 2.7 Hz, 1H), 7.71 (d, J=8.6 Hz, 2H),7.59-7.36 (m, 2H), 4.38-4.27 (m, 1H), 4.20-4.12 (m, 1H), 3.58-3.51 (m,1H), 3.40 (t, J=8.4 Hz, 1H), 3.32 (s, 3H), 3.05-2.88 (m, 5H), 2.26-2.13(m, 1H), 2.10-1.96 m, 1H), 1.90-1.75 (m, 2H).

3-{1-[4-((2R,5R)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A218”)

UPLC/MS 0.74 min, [M+H]⁺ 492;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.27-8.03 (m, 2H), 7.82 (dd, J=9.2, 2.7 Hz, 1H), 7.71 (d, J=8.6 Hz, 2H),7.59-7.36 (m, 2H), 4.38-4.27 (m, 1H), 4.20-4.12 (m, 1H), 3.58-3.51 (m,1H), 3.40 (t, J=8.4 Hz, 1H), 3.32 (s, 3H), 3.05-2.88 (m, 5H), 2.26-2.13(m, 1H), 2.10-1.96 m, 1H), 1.90-1.75 (m, 2H).

3-{1-[4-((2S,5S)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A219”)

UPLC/MS 0.75 min, [M+H]⁺ 510;

¹H NMR (300 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.28 (s, 1H), 8.86 (s, 1H),8.22-7.99 (m, 3H), 7.78-7.66 (m, 2H), 7.33 (dd, J=11.5, 7.1 Hz, 1H),4.38-4.27 (m, 1H), 4.20-4.12 (m, 1H), 3.58-3.51 (m, 1H), 3.40 (t, J=8.4Hz, 1H), 3.32 (s, 3H), 3.05-2.88 (m, 5H), 2.26-2.13 (m, 1H), 2.10-1.96m, 1H), 1.90-1.75 (m, 2H).

3-{1-[4-((2R,5R)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A220”)

UPLC/MS 0.76 min, [M+H]⁺ 510;

¹H NMR (300 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.28 (s, 1H), 8.86 (s, 1H),8.22-7.99 (m, 3H), 7.78-7.66 (m, 2H), 7.33 (dd, J=11.5, 7.1 Hz, 1H),4.38-4.27 (m, 1H), 4.20-4.12 (m, 1H), 3.58-3.51 (m, 1H), 3.40 (t, J=8.4Hz, 1H), 3.32 (s, 3H), 3.05-2.88 (m, 5H), 2.26-2.13 (m, 1H), 2.10-1.96m, 1H), 1.90-1.75 (m, 2H).

6,7-difluoro-3-(1-{4-[3-(2-morpholin-4-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A221”)

UPLC/MS 0.49 min, [M+H]⁺ 551;

¹H NMR (400 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.28 (s, 1H), 8.13-8.06 (m,3H), 7.78-7.73 (m, 2H), 7.33 (dd, J=11.4, 7.1 Hz, 1H), 4.23-3.93 (m,1H), 3.73-3.36 (m, 10H), 2.47-2.30 (m, 6H), 2.06-1.94 (m, 2H).

6-fluoro-7-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A222”)

6,7-difluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A223”)

HPLC/MS 1.54 min (A), [M+H]⁺ 510;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.27 (s, 1H), 8.85 (s, 1H),8.17-8.04 (m, 3H), 7.78-7.72 (m, 2H), 7.33 (dd, J=11.4, 7.1 Hz, 1H),3.73-3.37 (m, 9H), 3.36-3.18 (m, 5H), 2.56-2.41 (m, 1H), 2.06-1.90 (m,1H), 1.76-1.58 (m, 1H).

6-fluoro-3-(1-{4-[3-(2-pyrrolidin-1-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A224”)

UPLC/MS 0.49 min, [M+H]⁺ 517;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.32 (s, 1H), 8.88 (s, 1H),8.17-8.11 (m, 2H), 7.84-7.72 (m, 3H), 7.48 (dd, J=9.0, 4.9 Hz, 1H), 7.43(td, J=8.7, 2.8 Hz, 1H), 4.32-4.12 (m, 1H), 3.83-3.31 (m, 10H),3.21-2.98 (m, 3H), 2.21-1.76 (m, 5H).

6,7-difluoro-3-(1-{4-[3-(2-pyrrolidin-1-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A225”)

UPLC/MS 0.50 min, [M+H]⁺ 535;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.30 (s, 1H), 8.87 (s, 1H),8.17-8.06 (m, 2H), 8.02 (dd, J=10.9, 8.5 Hz, 1H), 7.82-7.76 m, 2H), 7.37(dd, J=11.4, 7.1 Hz, 1H), 4.32-4.12 (m, 1H), 3.83-3.31 (m, 10H),3.21-2.98 (m, 3H), 2.21-1.76 (m, 5H).

(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-3-carboxylicAcid Amide (“A226”)

UPLC/MS 0.59 min, [M+H]⁺ 447.

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.11-8.06 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.72 (m, 2H),7.53-7.34 (m, 3H), 6.99-6.91 (m, 1H), 3.77-3.45 (m, 4H), 3.05-2.91 (m,1H), 2.20-1.93 (m, 2H).

6-fluoro-3-{1-[4-((2S,4R)-4-hydroxy-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A227”)

MS [M+H]⁺ 450;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.87 (s, 1H),8.10 (d, J=8.5 Hz, 2H), 7.82 (dd, J=9.2, 2.7 Hz, 1H), 7.76 (d, J=8.5 Hz,2H), 7.53 -7.37 (m, 2H), 4.83 (d, J=3.1 Hz, 1H), 4.78 (t, J=5.9 Hz, 1H),4.31 (q, J=6.2, 5.2 Hz, 1H), 4.23 (br. s, 1H), 3.79-3.69 (m, 1H),3.67-3.52 (m, 2H), 3.26 (d, J=11.1 Hz, 1H), 2.14-2.01 (m, 1H), 1.98-1.85(m, 1H).

6-fluoro-3-{1-[4-(2-oxa-6-aza-spiro[3.5]nonane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A228”)

MS [M+H]⁺ 460;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.10 (d, J=8.4 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz, 1H), 7.61 (d, J=7.4 Hz,2H), 7.50 -7.37 (m, 2H), 4.49-3.98 (m, 4H), 3.88 (br. s, 1H), 3.60 (br.s, 2H), 3.33 (br. s, 1H), 1.94-1.79 (m, 2H), 1.58-1.37 (m, 2H).

6-fluoro-3-{1-[4-(2-oxa-7-aza-spiro[3.5]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A229”)

MS [M+H]⁺ 460;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.08 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.3, 2.6 Hz, 1H), 7.60 (d, J=8.6 Hz,2H), 7.50 -7.37 (m, 2H), 4.35 (s, 4H), 3.55 (br. s, 2H), 3.32 (br. s,2H), 1.83 (br. s, 4H).

6-fluoro-3-{1-[4-(4-oxetan-3-yl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A230”)

MS [M+H]⁺ 475;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.32-9.23 (m, 1H), 8.85 (s,1H), 8.09 (d, J=8.6 Hz, 2H), 7.79 (dd, J=9.2, 2.6 Hz, 1H), 7.63 (d,J=8.6 Hz, 2H), 7.55-7.30 (m, 2H), 4.55 (t, J=6.5 Hz, 2H), 4.46 (t, J=6.1Hz, 2H), 3.66 (br. s, 2H), 3.47 (p, J=6.3 Hz, 1H), 3.42 (br. s, 2H),2.32 (br. s, 4H).

3-{1-[4-(2,5-dioxa-8-aza-spiro[3.5]nonane-8-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A231”)

MS [M+H]⁺ 462;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.12 (d, J=8.1 Hz, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.67 (d, J=8.4 Hz,2H), 7.53 -7.33 (m, 2H), 4.60-4.12 (m, 4H), 4.03-3.32 (m, 6H).

4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-oxetan-3-yl-benzamide(“A232”)

MS [M+H]⁺ 406;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.33 (s, 1H), 9.26 (d, J=6.4Hz, 1H), 8.86 (s, 1H), 8.17 (d, J=8.8 Hz, 2H), 8.12 (d, J=8.8 Hz, 2H),7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.52-7.37 (m, 2H), 5.04 (ddt, J=14.0, 7.5,6.5 Hz, 1H), 4.80 (dd, J=7.5, 6.4 Hz, 2H), 4.63 (t, J=6.4 Hz, 2H).

6,7-difluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A233”)

HPLC/MS 1.54 min (A), [M+H]⁺ 510;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.27 (s, 1H), 8.85 (s, 1H),8.17-8.04 (m, 3H), 7.78-7.72 (m, 2H), 7.33 (dd, J=11.4, 7.1 Hz, 1H),3.73-3.37 (m, 8H), 3.36-3.18 (m, 5H), 2.56-2.41 (m, 1H), 2.06-1.90 (m,1H), 1.76-1.58 (m, 1H).

6-fluoro-3-{1-[4-(2-oxa-5-aza-spiro[3.4]octane-5-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A234”)

MS [M+H]⁺ 446;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.09 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.75 (d, J=8.6 Hz,2H), 7.55 -7.30 (m, 2H), 5.47 (d, J=5.1 Hz, 2H), 4.33 (d, J=5.2 Hz, 2H),3.39 (t, J=6.5 Hz, 2H), 2.34 (t, J=6.7 Hz, 2H), 1.71 (p, J=6.6 Hz, 2H).

6-fluoro-3-{1-[4-(2-oxa-6-aza-spiro[3.3]heptane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A235”)

MS [M+H]⁺ 432;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.11 (d, J=8.7 Hz, 2H), 7.84 (d, J=8.7 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz,1H), 7.50 -7.38 (m, 2H), 4.70 (s, 4H), 4.55 (s, 2H), 4.25 (s, 2H).

6-fluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A236”)

HPLC/MS 1.49 min (A), [M+H]⁺ 492;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.16-8.03 (m, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.78-7.72 (m, 2H),7.50-7.40 (m, 2H). 3.73-3.37 (m, 8H), 3.36-3.18 (m, 5H), 2.56-2.41 (m,1H), 2.06-1.90 (m, 1H), 1.76-1.58 (m, 1H).

3-{1-[4-((3R,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A237”)

UPLC/MS 0.65 min, [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.13-8.05 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.72 (m, 2H),7.51-7.39 (m, 2H), 4.03 (q, J=5.1 Hz, 1H), 3.98-3.90 (m, 1H), 3.70-3.61(m, 2H), 3.53-3.41 (m, 2H), 3.38 (s, 3H), 3.28 (s, 3H).

4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N,N-bis-(2-methoxy-ethyl)-benzamide (“A238”)

UPLC/MS 0.70 min, [M+H]⁺ 466;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.12-8.02 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.68-7.56 (m, 2H),7.51-7.39 (m, 2H), 3.75-3.11 (m, 14H).

3-{1-[4-(3-diethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A239”)

UPLC/MS 0.50 min, [M+H]⁺ 507;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.26 (s, 1H), 8.83 (s, 1H), 8.10 (s,1H, formate-H), 8.12-8.07 (m, 2H), 8.01 (dd, J=10.9, 8.5 Hz, 1H),7.78-7.72 (m, 2H), 7.33 (dd, J=11.4, 7.1 Hz, 1H), 3.90-3.47 (m, 4H),3.38-3.04 (m, 6H), 2.72-2.57 (m, 1H), 2.23-2.07 (m, 1H), 1.78-1.66 (m,1H), 1.28-1.11 (m, 6H).

N-(3-acetyl-3-aza-bicyclo[3.1.0]hex-6-yl)-4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide(“A240”)

MS [M+H]⁺ 473;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.32 (s, 1H), 8.87 (s, 1H),8.72 (d, J=3.9 Hz, 1H), 8.15 (d, J=8.7 Hz, 2H), 8.06 (d, J=8.7 Hz, 2H),7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.52-7.38 (m, 2H), 3.66 (qd, J=10.2, 4.1Hz, 2H), 3.44-3.32 (m, 2H), 2.60 (q, J=2.8 Hz, 1H), 1.94 (s, 3H),1.90-1.80 (m, 1H), 1.10 (t, J=7.0 Hz, 1H).

6-fluoro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A241”)

MS [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (s, 1H), 8.87 (s, 1H),8.11 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.76 (d, J=8.3 Hz,2H), 7.51 -7.40 (m, 2H), 4.81 (t, J=5.8 Hz, 1H), 4.24 (s, 1H), 3.92 (s,1H), 3.82-3.71 (m, 1H), 3.67-3.50 (m, 2H), 3.40 (d, J=11.8 Hz, 1H), 3.12(s, 3H), 2.18-2.03 (m, 2H).

(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-2-carboxylicacid amide (“A242”)

UPLC/MS 0.60 min, [M+H]⁺ 447;

mixture of rotamers, some signals of main rotamer: ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.11 (d, J=8.6 Hz,2H), 7.88-7.73 (m, 3H), 7.53-7.38 (m, 3H), 6.97 (bs, 1H), 4.40 (dd,J=8.3, 5.2 Hz, 1H), 3.75-3.56 (m, 2H), 2.26-2.16 (m, 1H), 1.95-1.75 (m,3H).

(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-3-carboxylicacid amide (“A243”)

UPLC/MS 0.60 min, [M+H]⁺ 447;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.29 (s, 1H), 8.85 (s, 1H),8.11-8.06 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.78-7.72 (m, 2H),7.53-7.34 (m, 3H), 6.99-6.91 (m, 1H), 3.77-3.45 (m, 4H), 3.05-2.91 (m,1H), 2.20-1.93 (m, 2H).

6-fluoro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A244”)

MS [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.28 (s, 1H), 9.29(s, 1H), 8.85 (s, 1H), 8.08 (d, J=8.3 Hz, 2H), 7.80 (dd, J=9.3, 2.7 Hz,1H), 7.73 (d, J=7.6 Hz, 2H), 7.51-7.37 (m, 2H), 4.83 (s, 0,7H), 4.70 (s,0,3H), 4.22 (br. s, 0,7H), 4.04 (br. s, 0,3H), 3.91 (br. s, 1H), 3.64(br. s, 2H), 3.48-3.36 (m, 1H), 3.22 (s, 3H), 2.26-2.11 (m, 1H),2.10-1.95 (m, 1H).

6-fluoro-3-{1-[4-(2-oxa-5-aza-spiro[3.5]nonane-5-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A245”)

MS [M+H]⁺ 460;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.12 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.74 (d, J=8.6 Hz,2H), 7.52 -7.35 (m, 2H), 4.71 (d, J=6.8 Hz, 2H), 4.38 (d, J=6.9 Hz, 2H),3.23 (t, J=5.5 Hz, 2H), 2.06 (t, J=6.0 Hz, 2H), 1.70 (p, J=6.0 Hz, 2H),1.26 (p, J=5.7 Hz, 2H).

6-chloro-3-{1-[4-((S)-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A246”)

MS [M+H]⁺ 450;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.28 (s, 1H), 8.84 (s, 1H),8.08 (d, J=8.4 Hz, 2H), 8.05 (d, J=2.2 Hz, 1H), 7.73 (d, J=8.0 Hz, 2H),7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 4.79 (t, J=5.4 Hz,1H), 4.17 (s, 1H), 3.60 (s, 2H), 3.48 (dt, J=10.2, 6.7 Hz, 1H), 3.36 (s,1H), 2.03-1.83 (m, 3H), 1.82-1.60 (m, 1H).

6-chloro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A247”)

MS [M+H]⁺ 480;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.33 (s, 1H), 9.28(s, 1H), 8.84 (s, 1H), 8.08 (d, J=8.4 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H),7.73 (d, J=8.1 Hz, 2H), 7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz,1H), 4.81 (br. s, 0,7H), 4.68 (br. s, 0,3H), 4.22 (br. s, 0,7H), 4.05(br. s, 0,3H), 3.90 (br. s, 1H), 3.64 (br. s, 2H), 3.49-3.35 (m, 1H),3.22 (s, 3H), 2.24-2.12 (m, 1H), 2.11-1.94 (m, 1H).

6-chloro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A248”)

MS [M+H]⁺ 480;

¹H NMR (500 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.29 (s, 1H), 8.84 (s, 1H),8.10 (d, J=8.4 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H), 7.75 (d, J=8.3 Hz, 2H),7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 4.80 (s, 1H), 4.24(s, 1H), 3.91 (q, J=4.2 Hz, 1H), 3.74 (d, J=11.2 Hz, 1H), 3.61 (dd,J=11.7, 3.7 Hz, 1H), 3.55 (d, J=11.2 Hz, 1H), 3.40 (d, J=11.7 Hz, 1H),3.11 (s, 3H), 2.08 (dd, J=8.2, 4.9 Hz, 2H).

6-chloro-3-(1-{4-[3-(4-hydroxy-piperidin-1-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A249”)

MS [M+H]⁺ 519;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.33 (s, 1H), 9.28(s, 1H), 8.84 (s, 1H), 8.07 (d, J=8.4 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H),7.75 (t, J=9.1 Hz, 2H), 7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz,1H), 4.53 (d, J=4.0 Hz, 0.5H), 4.50 (d, J=4.0 Hz, 0.5H), 3.83-3.37 (m,4H), 3.37-3.18 (m, 1H), 2.94-2.51 (m, 3H), 2.21-1.94 (m, 3H), 1.82-1.60(m, 3H), 1.47-1.27 (m, 2H).

6-chloro-3-{1-[4-(4-oxetan-3-yl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A250”)

MS [M+H]⁺ 491;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.27 (s, 1H), 8.84 (s, 1H),8.09 (d, J=8.6 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H), 7.63 (d, J=8.6 Hz, 2H),7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 4.55 (t, J=6.5 Hz,2H), 4.46 (t, J=6.1 Hz, 2H), 3.66 (br. s, 2H), 3.54-3.33 (m, 3H), 2.32(br. s, 4H).

6-fluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A251”)

HPLC/MS 1.46 min (A), [M+H]⁺ 478;

¹H NMR (500 MHz, DMSO-d6) mixture of 2 rotamers: δ 12.29 (s, 1H), 9.30(s, 1H), 8.86 (s, 1H), 8.15-8.05 (m, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H),7.78-7.72 (m, 0.5H), 7.54-7.38 (m, 2H), 4.21-4.17 (m, 0.5H), 4.13-4.08(m, 0.5H), 3.71-3.37 (m, 8H), 3.28 (s, 1.5H), 3.21 (s, 11.5H), 2.06-1.95(m, 2H).

6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A252”)

HPLC/MS 1.46 min (A), [M+H]⁺ 478;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers: δ 12.29 (s, 1H), 9.30(s, 1H), 8.86 (s, 1H), 8.15-8.05 (m, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H),7.78-7.72 (m, 0.5H), 7.54-7.38 (m, 2H), 4.21-4.17 (m, 0.5H), 4.13-4.08(m, 0.5H), 3.71-3.37 (m, 8H), 3.28 (s, 1.5H), 3.21 (s, 11.5H), 2.06-1.95(m, 2H).

6-chloro-3-{1-[4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A253”)

MS [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.33 (s, 1H), 9.28(s, 1H), 8.84 (s, 1H), 8.08 (d, J=8.6 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H),7.71 (d, J=8.4 Hz, 2H), 7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz,1H), 4.29 (br.s, 0.7H), 4.07 (br. s, 0.3H), 3.73-3.55 (m, 1H), 3.54-3.42(m, 2H), 3.32 (s, 3H), 3.16-2.92 (m, 1H), 2.09-1.96 (m, 1H), 1.96-1.81(m, 2H), 1.81-1.63 (m, 1H).

6-chloro-3-{1-[4-(3-dimethylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A254”)

MS [M+H]⁺ 463;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.33 (s, 1H), 9.28(s, 1H), 8.84 (s, 1H), 8.08 (d, J=8.6 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H),7.75 (t, J=8.0 Hz, 2H), 7.58 (dd, J=8.7, 2.4 Hz, 1H), 7.40 (d, J=8.8 Hz,1H), 3.79-3.71 (m, 0.5H), 3.70-3.61 (m, 0.5H), 3.60-3.43 (m, 2H),3.38-3.20 (m, 1H), 2.82 -2.61 (m, 1H), 2.20 (s, 3H), 2.11 (s, 3H),2.10-1.97 (m, 1H), 1.84-1.67 (m, 1H).

6-chloro-3-{1-[4-(2-hydroxymethyl-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A255”)

MS [M+H]⁺ 464;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.32 (s, 1H), 9.26(s, 1H), 8.84 (s, 1H), 8.12-7.99 (m, 3H), 7.65-7.52 (m, 3H), 7.40 (d,J=8.8 Hz, 1H), 4.79 (t, J=5.5 Hz, 1H), 4.73-4.52 (m, 0.3H), 4.52-4.15(m, 0.7H), 3.95-3.36 (m, 3H), 3.19-2.77 (m, 1H), 1.96-1.29 (m, 6H).

6-chloro-3-{1-[4-(2-oxa-7-aza-spiro[3.5]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A256”)

MS [M+H]⁺ 476;

¹H NMR (500 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.27 (s, 1H), 8.84 (s, 1H),8.08 (d, J=8.6 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H), 7.60 (d, J=8.5 Hz, 2H),7.58 (d, J=2.4 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 4.35 (br. s, 4H), 3.55(br. s, 2H), 3.27 (br. s, 2H), 1.83 (br. s, 4H).

6-chloro-3-{1-[4-(2-oxa-6-aza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A257”)

MS [M+H]⁺ 462;

¹H NMR (500 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.28 (d, J=2.4 Hz, 1H), 8.84(s, 1H), 8.09 (t, J=7.7 Hz, 2H), 8.05 (d, J=2.0 Hz, 1H), 7.75 (dd,J=8.4, 4.2 Hz, 2H), 7.58 (dd, J=8.8, 2.4 Hz, 1H), 7.41 (d, J=8.8 Hz,1H), 4.64 (d, J=6.0 Hz, 1H), 4.55-4.42 (m, 3H), 3.73 (d, J=14.1 Hz, 2H),3.50 (dt, J=14.7, 6.9 Hz, 2H), 2.18 (dt, J=12.8, 7.0 Hz, 2H).

6-chloro-3-{1-[4-(2-oxa-6-aza-spiro[3.3]heptane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A258”)

MS [M+H]⁺ 448;

¹H NMR (500 MHz, DMSO-d₆) δ ¹H NMR (500 MHz, DMSO-d₆) δ 12.33 (s, 1H),9.29 (s, 1H), 8.84 (s, 1H), 8.10 (d, J=8.7 Hz, 2H), 8.05 (d, J=2.3 Hz,1H), 7.84 (d, J=8.7 Hz, 2H), 7.58 (dd, J=8.7, 2.4 Hz, 1H), 7.40 (d,J=8.8 Hz, 1H), 4.70 (s, 4H), 4.55 (s, 2H), 4.25 (s, 2H).

6-chloro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A259”)

HPLC/MS 1.56 min (A), [M+H]⁺ 494;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers: δ 12.33 (s, 1H), 9.29(s, 1H), 8.85 (s, 1H), 8.09 (d, J=8.3 Hz, 2H), 8.06 (d, J=2.4 Hz, 1H),7.76 (d, J=8.3 Hz, 2H), 7.59 (dd, J=8.8, 2.3 Hz, 1H), 7.41 (d, J=8.8 Hz,1H), 4.22-4.15 (m, 0.5H), 4.13-4.07 (m, 0.5H), 3.74-3.35 (m, 8H), 3.28(s, 1.5H), 3.21 (s, 1.5H), 2.12-1.88 (m, 2H).

6-chloro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A260”)

HPLC/MS 1.56 min (A), [M+H]⁺ 494;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers: δ 12.33 (s, 1H), 9.29(s, 1H), 8.85 (s, 1H), 8.09 (d, J=8.3 Hz, 2H), 8.06 (d, J=2.4 Hz, 1H),7.76 (d, J=8.3 Hz, 2H), 7.59 (dd, J=8.8, 2.3 Hz, 1H), 7.41 (d, J=8.8 Hz,1H), 4.22-4.15 (m, 0.5H), 4.13-4.07 (m, 0.5H), 3.74-3.35 (m, 8H), 3.28(s, 1.5H), 3.21 (s, 1.5H), 2.12-1.88 (m, 2H).

6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-pyrazol-4-yl)-1H-quinolin-2-one(“A261”)

HPLC/MS 1.46 min (A), [M+H]⁺ 477;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.12 (s, 1H), 9.20(s, 1H), 8.47 (s, 1H), 8.42 (s, 1H), 8.01-7.91 (m, 2H), 7.70 (d, J=8.4Hz, 2H), 7.49 (dt, J=9.3, 1.7 Hz, 1H), 7.44-7.35 (m, 2H), 4.21-4.14 (m,0.5H), 4.13-4.06 (m, 0.5H), 3.75-3.35 (m, 7H), 3.28 (s, 1.5H), 3.21 (s,1.5H), 2.05-1.93 (m, 2H).

(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-2-carboxylicacid amide (“A262”)

UPLC/MS 0.62 min, [M+H]⁺ 447;

mixture of rotamers, some signals of main rotamer: ¹H NMR (400 MHz,DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.11 (d, J=8.6 Hz,2H), 7.88-7.73 (m, 3H), 7.53-7.38 (m, 3H), 6.97 (bs, 1H), 4.40 (dd,J=8.3, 5.2 Hz, 1H), 3.75-3.56 (m, 2H), 2.26-2.16 (m, 1H), 1.95-1.75 (m,3H).

3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A263”)

HPLC/MS 1.49 min (A), [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.13-8.06 (m, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.79-7.73 (m, 2H),7.52-7.39 (m, 2H), 3.97-3.92 (m, 1H), 3.91-3.87 (m, 1H), 3.76-3.62 (m,2H), 3.56 (d, J=13.4 Hz, 1H), 3.43 (d, J=11.7 Hz, 1H), 3.36 (s, 3H),3.26 (s, 3H).

3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A264”)

HPLC/MS 1.49 min (A), [M+H]⁺ 464;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.13-8.06 (m, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.79-7.73 (m, 2H),7.52-7.39 (m, 2H), 3.97-3.92 (m, 1H), 3.91-3.87 (m, 1H), 3.76-3.62 (m,2H), 3.56 (d, J=13.4 Hz, 1H), 3.43 (d, J=11.7 Hz, 1H), 3.36 (s, 3H),3.26 (s, 3H).

6-fluoro-3-{1-[4-((S)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A265”)

MS [M+H]⁺ 422;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.11 (d, J=8.6 Hz, 2H), 7.81 (dd, J=9.2, 2.4 Hz, 2H), 7.77 (d, J=8.4 Hz,1H), 7.50 -7.40 (m, 2H), 5.38 (dd, J=52.9, 40.3 Hz, 1H), 3.94-3.52 (m,4H), 2.30-2.02 (m, 2H).

6-chloro-3-{1-[4-((S)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A266”)

MS [M+H]⁺ 438;

¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.11 (d, J=8.6 Hz, 2H), 8.06 (d, J=2.3 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H),7.77 (d, J=8.3 Hz, 1H), 7.60 (dd, J=8.8, 2.4 Hz, 1H), 7.42 (d, J=8.8 Hz,1H), 5.53-5.23 (m, 1H), 3.94-3.52 (m, 4H), 2.30-2.00 (m, 2H).

3-{1-[4-(3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A267”)

MS [M+H]⁺ 440;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.12 (d, J=8.6 Hz, 2H), 7.84-7.76 (m, 3H), 7.50-7.40 (m, 2H), 3.96 (t,J=13.2 Hz, 2H), 3.76 (br. s, 2H), 2.48 (br. s, 2H).

6-chloro-3-{1-[4-(3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A268”)

MS [M+H]⁺ 440;

¹H NMR (500 MHz, DMSO-d₆) δ ¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H),9.31 (s, 1H), 8.86 (s, 1H), 8.12 (d, J=8.6 Hz, 2H), 8.07 (d, J=2.4 Hz,1H), 7.81 (d, J=8.2 Hz, 2H), 7.60 (dd, J=8.8, 2.4 Hz, 1H), 7.42 (d,J=8.8 Hz, 1H), 3.96 (t, J=13.2 Hz, 2H), 3.76 (br. s, 2H), 2.48 (br.s,2H).

6-fluoro-3-{1-[4-((R)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A269”)

MS [M+H]⁺ 421;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.09 (d, J=8.6 Hz, 2H), 7.83-7.74 (m, 3H), 7.50-7.41 (m, 2H), 5.52-5.20(m, 1H), 3.91-3.58 (m, 4H), 2.29-2.02 (m, 2H).

6-chloro-3-{1-[4-((R)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A270”)

MS [M+H]⁺ 438;

¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.11 (d, J=8.6 Hz, 2H), 8.06 (d, J=2.3 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H),7.77 (d, J=8.3 Hz, 1H), 7.60 (dd, J=8.8, 2.4 Hz, 1H), 7.42 (d, J=8.8 Hz,1H), 5.53-5.23 (m, 1H), 3.94-3.52 (m, 4H), 2.30-2.00 (m, 2H).

6-chloro-3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A271”)

HPLC/MS 1.60 min (A), [M+H]⁺ 480;

1H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.13-8.07 (m, 2H), 8.06 (d, J=2.4 Hz, 1H), 7.81-7.73 (m, 2H), 7.60 (dd,J=8.8, 2.4 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 3.94 (bs, 1H), 3.89 (bs,1H), 3.69 (td, J=14.3, 13.2, 4.5 Hz, 2H), 3.56 (d, J=13.4 Hz, 1H), 3.43(d, J=11.7 Hz, 1H), 3.37 (s, 3H), 3.26 (s, 3H).

6-chloro-3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A272”)

HPLC/MS 1.59 min (A), [M+H]⁺ 480;

1H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.13-8.07 (m, 2H), 8.06 (d, J=2.4 Hz, 1H), 7.81-7.73 (m, 2H), 7.60 (dd,J=8.8, 2.4 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 3.94 (bs, 1H), 3.89 (bs,1H), 3.69 (td, J=14.3, 13.2, 4.5 Hz, 2H), 3.56 (d, J=13.4 Hz, 1H), 3.43(d, J=11.7 Hz, 1H), 3.37 (s, 3H), 3.26 (s, 3H).

6-fluoro-3-{1-[4-(pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A273”)

UPLC/MS 0.72 min, [M+H]⁺ 404;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.18-8.03 (m, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.79-7.68 (m, 2H),7.54-7.37 (m, 2H), 3.51 (t, J=6.7 Hz, 2H), 3.46 (t, J=6.3 Hz, 2H),1.95-1.81 (m, 4H).

6-fluoro-3-{1-[4-((R)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A274”)

MS [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.12 (d, J=8.7 Hz, 2H), 7.92 (d, J=8.7 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz,1H), 7.50 -7.39 (m, 2H), 5.49 (d, J=4.0 Hz, 1H), 4.71 (dt, J=6.1, 4.1Hz, 1H), 4.03-3.91 (m, 2H), 3.87 (d, J=1.7 Hz, 1H), 3.66 (dd, J=11.5,1.6 Hz, 1H).6-chloro-3-{1-[4-((R)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A275”)

MS [M+H]⁺ 438;

¹H NMR (400 MHz, DMSO-d₆) δ δ 12.33 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.12 (d, J=8.8 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H), 7.92 (d, J=8.7 Hz, 2H),7.59 (dd, J=8.8, 2.4 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 5.49 (d, J=4.0 Hz,1H), 4.77-4.62 (m, 1H), 4.03-3.91 (m, 2H), 3.86 (dd, J=8.6, 1.8 Hz, 1H),3.66 (dd, J=11.4, 1.6 Hz, 1H).

6-fluoro-3-{1-[4-((S)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A276”)

MS [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.12 (d, J=8.7 Hz, 2H), 7.92 (d, J=8.7 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz,1H), 7.50 -7.39 (m, 2H), 5.49 (d, J=4.0 Hz, 1H), 4.71 (dt, J=6.1, 4.1Hz, 1H), 4.03-3.91 (m, 2H), 3.87 (d, J=1.7 Hz, 1H), 3.66 (dd, J=11.5,1.6 Hz, 1H).

6-chloro-3-{1-[4-((S)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A277”)

MS [M+H]⁺ 438;

¹H NMR (400 MHz, DMSO-d₆) δ δ 12.33 (s, 1H), 9.30 (s, 1H), 8.85 (s, 1H),8.12 (d, J=8.8 Hz, 2H), 8.05 (d, J=2.3 Hz, 1H), 7.92 (d, J=8.7 Hz, 2H),7.59 (dd, J=8.8, 2.4 Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 5.49 (d, J=4.0 Hz,1H), 4.77-4.62 (m, 1H), 4.03-3.91 (m, 2H), 3.86 (dd, J=8.6, 1.8 Hz, 1H),3.66 (dd, J=11.4, 1.6 Hz, 1H).

6-fluoro-3-{1-[4-((R)-2-pyrrolidin-1-ylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A278”)

HPLC/MS 1.28 min (A), [M+H]⁺ 487;

¹H NMR (500 MHz, DMSO-d₆) δ 12.22 (s, 1H), 9.22 (s, 1H), 8.79 (s, 1H),8.07-7.97 (m, 2H), 7.74 (dd, J=9.2, 2.7 Hz, 1H), 7.70-7.60 (m, 2H),7.49-7.30 (m, 2H), 4.34-3.88 (m, 1H), 3.61-3.28 (m, 3H), 2.78-2.02 (m,6H), 2.00-1.90 (m, 1H), 1.90-1.76 (m, 2H), 1.76-1.32 (m, 4H).

6-fluoro-3-{1-[4-((S)-2-pyrrolidin-1-ylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A279”)

HPLC/MS 1.29 min (A), [M+H]⁺ 487;

¹H NMR (500 MHz, DMSO-d₆) δ 12.22 (s, 1H), 9.22 (s, 1H), 8.79 (s, 1H),8.07-7.97 (m, 2H), 7.74 (dd, J=9.2, 2.7 Hz, 1H), 7.70-7.60 (m, 2H),7.49-7.30 (m, 2H), 4.34-3.88 (m, 1H), 3.61-3.28 (m, 3H), 2.78-2.02 (m,6H), 2.00-1.90 (m, 1H), 1.90-1.76 (m, 2H), 1.76-1.32 (m, 4H).

3-{1-[4-(azetidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A280”)

UPLC/MS 0.70 min, [M+H]⁺ 390;

¹H NMR (400 MHz, DMSO-d₆) δ 12.26 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H),8.22-8.00 (m, 2H), 7.94-7.84 (m, 2H), 7.81 (dd, J=9.3, 2.6 Hz, 1H),7.54-7.38 (m, 2H), 4.38 (t, J=7.4 Hz, 2H), 4.10 (t, J=7.8 Hz, 2H),2.38-2.18 (m, 2H).

6-fluoro-3-(1-{4-[2-(4-methyl-piperazine-1-carbonyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A281”)

UPLC/MS 0.49 min, [M+H]⁺ 530;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.20 (s, 1H), 8.76 (s, 1H), 8.00 (d,J=8.6 Hz, 2H), 7.69 (d, J=8.3 Hz, 2H), 7.56 (dd, J=9.1, 2.8 Hz, 1H),7.39 (dd, J=9.1, 4.7 Hz, 1H), 7.26 (td, J=8.8, 2.8 Hz, 1H), 5.06-4.70(m, 2H), 4.60-4.19 (m, 3H), 3.78-2.85 (m, 6H), 2.82 (s, 3H), 2.31-2.15(m, 2H), 2.03-1.70 (m, 2H).

6-fluoro-3-{1-[4-((R)-3-methanesulfonyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A282”)

HPLC/MS 1.41 min (A), [M+H]⁺ 482;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.12 (d, J=8.4 Hz, 2H), 7.88-7.70 (m, 3H), 7.53-7.40 (m, 2H), 4.15-3.55(m, 5H), 3.13-2.99 (m, 3H), 2.43-2.20 (m, 2H).

6-fluoro-3-{1-[4-((S)-3-methanesulfonyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A283”)

HPLC/MS 1.40 min (A), [M+H]⁺ 482;

¹H NMR (400 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.31 (s, 1H), 8.86 (s, 1H),8.12 (d, J=8.4 Hz, 2H), 7.88-7.70 (m, 3H), 7.53-7.40 (m, 2H), 4.15-3.55(m, 5H), 3.13-2.99 (m, 3H), 2.43-2.20 (m, 2H).

6-fluoro-3-{1-[4-(3-methanesulfonylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A284”)

UPLC/MS 0.65 min, [M+H]⁺ 496;

¹H NMR (700 MHz, DMSO-d₆) 1:1 mixture of rotamers, selected peaks δ12.30 (s, 1H), 9.31 (s, 0.5H), 9.30 (s, 0.5H), 8.86 (s, 1H), 8.13-8.08(m, 2H), 7.81 (dd, J=9.1, 2.9 Hz, 1H), 7.79-7.71 (m, 2H), 7.47 (td,J=8.8, 2.8 Hz, 1H), 7.43 (dd, J=9.0, 4.8 Hz, 1H), 3.05 (s, 1.5H), 2.98(s, 1.5H).

6-fluoro-3-(1-{4-[2-(1-methyl-1H-pyrazol-4-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A285”)

MS [M+H]⁺ 484;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.32 (s, 1H), 9.31(s, 0,70H), 9.26 (s, 0,30H), 8.86 (s, 1H), 8.09 (d, J=8.1 Hz, 1,4H),7.97 (d, J=8.1 Hz, 0,60H), 7.81 (d, J=9.1 Hz, 1H), 7.76 (d, J=8.4 Hz,2H), 7.68 (s, 1H), 5.26 -5.14 (m, 0,70H), 4.99-4.87 (m, 0,30H), 3.80 (s,2H), 3.72 (s, 1H), 3.71-3.61 (m, 1,40H), 3.46-3.38 (m, 0,6H), 2.29-2.13(m, 1H), 2.02-1.75 (m, 3H).

6-fluoro-3-{1-[4-(2-pyridin-3-yl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A286”)

MS [M+H]⁺ 481;

¹H NMR (500 MHz, DMSO-d₆) mixture of rotamers, signals of major δ 12.32(s, 1H), 9.32 (s, 1H), 8.87 (s, 1H), 8.57 (d, J=91.1 Hz, 2H), 8.12 (d,J=8.5 Hz, 2H), 7.90-7.85 (m, 2H), 7.84-7.78 (m, 2H), 7.54-7.31 (m, 3H),5.18 (t, J=6.9 Hz, 1H), 3.98-3.89 (m, 1H), 3.62-3.54 (m, 1H), 2.49-2.39(m, 1H), 2.03 -1.74 (m, 3H).

6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-ylmethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A287”)

MS [M+H]⁺ 516;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.33 (s, 1H), 8.87 (s, 1H), 8.15 (d,J=8.6 Hz, 2H), 7.86 (d, J=8.4 Hz, 2H), 7.78 (dd, J=9.3, 2.7 Hz, 1H),7.50-7.39 (m, 2H), 4.70-4.60 (m, 1H), 4.35-3.30 (m, 12H), 2.93 (s, 3H),2.30-2.16 (m, 1H), 2.03-1.73 (m, 3H).

6-fluoro-3-{1-[4-(2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A288”)

UPLC/MS 0.76 min, [M+H]⁺ 418;

¹H NMR (500 MHz, DMSO-d₆) mixture of rotamers, signals of major rotamer:δ 12.31 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.26-7.95 (m, 2H), 7.82(dd, J=9.2, 2.8 Hz, 1H), 7.73 (d, J=8.1 Hz, 2H), 7.47 (td, J=8.8, 2.8Hz, 1H), 7.43 (dd, J=9.0, 4.9 Hz, 1H), 4.25-4.14 (m, 1H), 3.57-3.51 (m,1H), 3.37-3.32 (m, 1H), 2.10 (dq, J=13.4, 6.8 Hz, 1H), 1.99-1.84 (m,1H), 1.79-1.68 (m, 1H), 1.64-1.53 (m, 1H), 1.29 (d, J=6.2 Hz, 3H).

6-fluoro-3-{1-[4-(2-methyl-2,6-diaza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A289”)

UPLC/MS 0.47 min, [M+H]⁺ 459;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers δ 12.33 (s, 1H), 9.89(bs, 1H, NH⁺), 9.32 (s, 0.5H), 9.31 (s, 0.5H), 8.86 (s, 1H), 8.20-8.04(m, 2H), 7.82 (dd, J=9.2, 2.8 Hz, 1H), 7.79-7.74 (m, 2H), 7.48 (ddd,J=9.2, 6.1, 2.3 Hz, 1H), 7.43 (dd, J=8.8, 4.6 Hz, 1H), 4.26-3.94 (m,4H), 3.79-3.69 (m, 2H), 3.59-3.48 (m, 2H), 2.87 (s, 1.5H), 2.78 (s,1.5H), 2.24-2.13 (m, 2H).

6-chloro-3-{1-[4-(2-methyl-2,6-diaza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A290”)

UPLC/MS 0.50 min, [M+H]⁺ 475;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers δ 12.38 (s, 1H), 9.83(bs, 1H, NH⁺), 9.32 (s, 0.5H), 9.31 (s, 0.5H), 8.86 (s, 1H), 8.17-8.09(m, 2H), 8.08 (d, J=2.3 Hz, 1H), 7.78-7.74 (m, 2H), 7.61 (dt, J=8.8, 1.8Hz, 1H), 7.41 (d, J=8.8 Hz, 1H), 4.26-3.94 (m, 4H), 3.79-3.69 (m, 2H),3.59-3.48 (m, 2H), 2.84 (s, 1.5H), 2.75 (s, 1.5H), 2.24-2.13 (m, 2H).

6-fluoro-3-{1-[4-((3aR,6aR)-5-methyl-hexahydro-pyrrolo[3,4-b]pyrrole-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A291”)

HPLC/MS 1.23 min (A), [M+H]⁺ 459;

¹H NMR (500 MHz, DMSO-d₆) mixture of rotamers, signals of major rotamer:δ 12.33 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.18-8.02 (m, 2H), 7.82(dd, J=9.2, 2.8 Hz, 1H), 7.75-7.70 (m, 1H), 7.47 (td, J=8.8, 2.8 Hz,1H), 7.42 (dd, J=9.0, 4.9 Hz, 1H), 4.56 (ddd, J=8.1, 5.8, 2.2 Hz, 1H),3.62 (td, J=10.3, 6.6 Hz, 1H), 3.46 (ddd, J=10.5, 8.0, 2.7 Hz, 1H),2.95-2.80 (m, 1H), 2.74 (dd, J=9.9, 2.2 Hz, 1H), 2.57-2.51 (m, 2H),2.47-2.36 (m, 1H), 2.24 (s, 3H), 2.02-1.88 (m, 1H), 1.74 (ddd, J=12.1,6.0, 2.8 Hz, 1H).

6-chloro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A292”)

HPLC/MS 1.69 min (A), [M+H]⁺ 434;

¹H NMR (500 MHz, DMSO-d₆) mixture of rotamers, signals of major rotamer:δ 12.37 (s, 1H), 9.30 (s, 1H), 8.86 (s, 1H), 8.10-8.07 (m, 2H), 8.07 (d,J=2.4 Hz, 1H), 7.73 (d, J=8.3 Hz, 1H), 7.60 (dd, J=8.8, 2.4 Hz, 1H),7.40 (d, J=8.8 Hz, 1H), 4.18 (h, J=5.9 Hz, 1H), 3.58-3.50 (m, 1H),3.39-3.32 (m, 1H), 2.10 (dq, J=13.3, 6.8 Hz, 1H), 1.85-1.85 (m, 1H),1.78-1.67 (m, 1H), 1.57 (dq, J=13.4, 6.8 Hz, 1H), 1.28 (d, J=6.2 Hz,2H).

3-{1-[4-(2,2-dimethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A293”)

HPLC/MS 1.68 min (A), [M+H]⁺ 432;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.27 (s, 1H), 8.85 (s, 1H),8.05 (d, J=8.5 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz, 1H), 7.64 (d, J=8.3 Hz,2H), 7.53 -7.37 (m, 2H), 3.40 (t, J=6.5 Hz, 2H), 1.90-1.71 (m, 4H), 1.53(s, 6H).

6-fluoro-3-(1-{4-[3-(4-methyl-piperazine-1-carbonyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one(“A294”)

UPLC/MS 0.47 min, [M+H]⁺ 530;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers, selection of signalsδ 12.31 (s, 1H), 9.32 (s, 1H), 8.84 (s, 1H), 8.15-8.04 (m, 2H),7.85-7.67 (m, 3H), 7.50-7.34 (m, 2H), 2.20 (s, 1.5H), 2.15 (s, 1.5H).

Example 196-fluoro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A295”)

To a solution of methyl 4-(1H-pyrazol)-1-yl)-benzenecarboxylate (9.58 g,47.4 mmol) in acetic acid (100 ml) is added N-bromosuccinimide (9.00 g,50.6 mmol). The reaction mixture is heated to 100° C. and stirred atthis temperature for 2 hours. The reaction mixture is allowed to reachroom temperature. The solid is filtered off, washed with water and driedunder vacuum to afford methyl 4-(4-bromo-1H-pyrazol-1-yl)benzoate aswhite crystalline solid; UPLC/MS 0.82 min, [M+H]+ 281/283.

¹H NMR (400 MHz, DMSO-d₆) δ 8.94 (s, 1H), 8.17-8.06 (m, 2H), 8.03-7.98(m, 2H), 7.97 (s, 1H), 3.88 (s, 3H).

A suspension of methyl 4-(4-bromo-1H-pyrazol-1-yl)benzoate (5.12 g, 18.2mmol), bis(pinacolato)diboron (6.10 g, 24.0 mmol) and dry potassiumacetate (5.36 g, 54.6 mmol) in THF (110 ml) is flushed with nitrogen andbis(triphenyl-phosphine)palladium(II)chloride (260 mg, 0.37 mmol) isadded. The reaction mixture is heated to 65° C. under nitrogen andstirred at this temperature for 3 days. The reaction mixture is filteredover kieselguhr and washed with dichloromethane. The filtrate isevaporated and chromatographed on a silica gel column withcyclohexane/ethyl acetate as eluent to afford4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-benzoicacid methyl ester as white solid; UPLC/MS 0.86 min, [M+H]+ 329.

¹H NMR (300 MHz, DMSO-d₆) δ 8.87 (s, 1H), 8.11-8.03 (m, 4H), 7.93 (s,1H), 3.88 (s, 3H), 1.30 (s, 12H).

A suspension of 3-bromo-6-fluoro-1H-quinolin-2-one (980 mg, 4.05 mmol),4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-benzoicacid methyl ester (1.46 g, 4.45 mmol) and 645 mg (6.44 mmol) potassiumhydrogen carbonate in DMF (13 ml) and water (6.5 ml) is flushed withnitrogen and bis(triphenylphosphine)palladium(II)chloride (60 mg, 0.085mmol) is added. The mixture is irradiated in a microwave reactor for 1hour at 120° C. The reaction mixture is allowed to reach roomtemperature. The solids are filtered off, washed with water and methanoland dried under vacuum to afford4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-pyrazol-1-yl]-benzoicacid methyl ester as grey solid; UPLC/MS 0.80 min, [M+H]+ 364.

¹H NMR (400 MHz, DMSO-d₆) δ 12.14 (s, 1H), 9.25 (s, 1H), 8.51 (s, 1H),8.44 (s, 1H), 8.14-8.10 (m, 2H), 8.09-8.04 (m, 2H), 7.54-7.47 (m, 1H),7.45-7.35 (m, 2H), 3.89 (s, 3H).

To a solution of4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-pyrazol-1-yl]-benzoicacid methyl ester (832 mg, 2.29 mmol) in methanol (18 ml) is addedaqueous 2 M sodium hydroxide solution (9.5 ml, 19 mmol) and the reactionmixture is stirred for 1 hour at 80° C. The reaction mixture is allowedto reach room temperature and is acidified with 2 N HCl. The resultantprecipitate is filtered off, washed with water and dried under vacuum toafford4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-pyrazol-1-yl]-benzoicacid as grey solid; UPLC/MS 0.70 min, [M+H]⁺ 350.

To a suspension of4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-pyrazol-1-yl]-benzoicacid (28.0.0 mg, 0.08 mmol) in a mixture of 1,4-dioxane (0.4 ml) and DMF(0.4 ml) are added (R)-2-methylpyrrolidine p-toluenesulfonate (25.5 mg,0.10 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride(23.0 mg, 0.12 mmol), 1-hydroxybenzotriazole hydrate (10.8 mg, 0.08mmol) and 4-methylmorpholine (13.2 μl, 0.12 mmol). The resultantsuspension is stirred at room temperature for 2 hours. The reactionmixture is poured into water. The resultant precipitate is filtered off,washed with water and dried. The residue is chromatographed on a silicagel column with dichloromethane/methanol as eluent to afford6-fluoro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-oneas white crystals; HPLC/MS 1.60 min (A), [M+H]⁺ 417.

¹H NMR (500 MHz, DMSO-d₆), mixture of rotamers; main rotamer: δ 12.15(s, 1H), 9.20 (s, 1H), 8.47 (s, 1H), 8.42 (s, 1H), 8.00-7.92 (m, 2H),7.67 (d, J=8.2 Hz, 2H), 7.49 (dd, J=9.0, 2.5 Hz, 1H), 7.43-7.35 (m, 2H),4.20-4.11 (m, 1H), 3.59-3.50 (m, 1H), 3.42-3.34 (m, 1H), 2.09 (dq,J=12.6, 6.2, 5.7 Hz, 1H), 2.00-1.82 (m, 1H), 1.77-1.66 (m, 1H),1.63-1.51 (m, 1H), 1.27 (d, J=6.2 Hz, 3H).

The following compounds are prepared similarly:

6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A296”)

UPLC/MS 0.47 mm, [M+H]⁺ 432;

¹H NMR (400 MHz, DMSO-d₆) δ 12.11 (s, 1H), 9.18 (s, 1H), 8.46 (s, 1H),8.41 (s, 1H), 8.01-7.90 (m, 2H), 7.61-7.52 (m, 2H), 7.52-7.46 (m, 1H),7.41-7.37 (m, 2H), 3.5 (bs, 4H), 2.36 (bs, 4H), 2.22 (s, 3H).

6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A297”)

UPLC/MS 0.69 min, [M+H]⁺ 433;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.12 (s, 1H), 9.19(s, 1H), 8.47 (s, 1H), 8.41 (s, 1H), 7.95 (d, J=8.2 Hz, 2H), 7.78-7.62(m, 2H), 7.49 (dt, J=9.1, 1.7 Hz, 1H), 7.42-7.36 (m, 2H), 4.07-4.00 (m,0.5H), 3.99-3.93 (m, 0.5H), 3.71-3.40 (m, 4H), 3.29 (s, 1.5H), 3.19 (s,1.5H), 2.13-1.87 (m, 2H).

6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A298”)

UPLC/MS 0.69 min, [M+H]⁺ 433;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.12 (s, 1H), 9.19(s, 1H), 8.47 (s, 1H), 8.41 (s, 1H), 7.95 (d, J=8.2 Hz, 2H), 7.78-7.62(m, 2H), 7.49 (dt, J=9.1, 1.7 Hz, 1H), 7.42-7.36 (m, 2H), 4.07-4.00 (m,0.5H), 3.99-3.93 (m, 0.5H), 3.71-3.40 (m, 4H), 3.29 (s, 1.5H), 3.19 (s,1.5H), 2.13-1.87 (m, 2H).

6-fluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-pyrazol-4-yl)-1H-quinolin-2-one(“A299”)

UPLC/MS 0.69 min, [M+H]⁺ 477;

¹H NMR (400 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.12 (s, 1H), 9.19(s, 1H), 8.47 (s, 1H), 8.42 (s, 1H), 7.95 (d, J=8.5 Hz, 2H), 7.70 (d,J=8.4 Hz, 2H), 7.49 (dt, J=9.1, 1.7 Hz, 1H), 7.44-7.34 (m, 2H),4.22-4.14 (m, 0.5H), 4.13-4.06 (m, 0.5H), 3.73-3.36 (m, 8H), 3.28 (s,1.5H), 3.21 (s, 1.5H), 2.06-1.90 (m, 2H).

3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A300”)

HPLC/MS 1.50 min (A), [M+H]⁺ 463;

¹H NMR (700 MHz, DMSO-d₆) δ 12.14 (s, 1H), 9.21 (s, 1H), 8.48 (s, 1H),8.43 (s, 1H), 8.00-7.93 (m, 2H), 7.74-7.67 (m, 2H), 7.50 (dd, J=9.0, 2.5Hz, 1H), 7.44-7.34 (m, 2H), 3.94 (d, J=4.7 Hz, 1H), 3.91-3.86 (m, 1H),3.72 (dd, J=11.8, 4.3 Hz, 1H), 3.65 (dd, J=13.3, 4.9 Hz, 1H), 3.55 (d,J=13.4 Hz, 1H), 3.44 (d, J=11.7 Hz, 1H), 3.36 (s, 3H), 3.25 (s, 3H).

6-fluoro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A301”)

MS [M+H]⁺ 463;

¹H NMR (500 MHz, DMSO-d₆) δ 12.11 (s, 1H), 9.19 (s, 1H), 8.46 (s, 1H),8.41 (s, 1H), 7.96 (d, J=8.4 Hz, 2H), 7.68 (d, J=8.2 Hz, 2H), 7.49 (dt,J=9.2, 1.5 Hz, 1H), 7.39 (dd, J=7.5, 2.0 Hz, 2H), 4.79 (t, J=5.8 Hz,1H), 4.23 (br. s, 1H), 3.90 (br. s, 1H), 3.78-3.67 (m, 1H), 3.61 (dd,J=11.8, 3.6 Hz, 1H), 3.59-3.50 (m, 1H), 3.42 (d, J=11.7 Hz, 1H), 3.17(d, J=5.2 Hz, 2H), 3.10 (s, 3H) 2.17-1.99 (m, 2H).

6-fluoro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A302”)

MS [M+H]⁺ 463;

¹H NMR (500 MHz, DMSO-d₆) δ 12.11 (s, 1H), 9.19 (s, 1H), 8.46 (s, 1H),8.41 (s, 1H), 7.94 (d, J=8.6 Hz, 2H), 7.67 (d, J=8.2 Hz, 2H), 7.49 (dt,J=9.2, 1.5 Hz, 1H), 7.41-7.37 (m, 2H), 4.81 (br. s, 1H), 4.22 (br. s,1H), 3.90 (br. s, 1H), 3.76-3.48 (m, 2H), 3.41 (dd, J=11.3, 5.0 Hz, 1H),3.22 (s, 3H), 3.17 (d, J=5.2 Hz, 1H), 2.16 (d, J=8.3 Hz, 1H), 2.02 (s,1H).

3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A303”)

HPLC/MS 1.50 min (A), [M+H]⁺ 463;

¹H NMR (700 MHz, DMSO-d₆) δ 12.14 (s, 1H), 9.21 (s, 1H), 8.48 (s, 1H),8.43 (s, 1H), 8.00-7.93 (m, 2H), 7.74-7.67 (m, 2H), 7.50 (dd, J=9.0, 2.5Hz, 1H), 7.44-7.34 (m, 2H), 3.94 (d, J=4.7 Hz, 1H), 3.91-3.86 (m, 1H),3.72 (dd, J=11.8, 4.3 Hz, 1H), 3.65 (dd, J=13.3, 4.9 Hz, 1H), 3.55 (d,J=13.4 Hz, 1H), 3.44 (d, J=11.7 Hz, 1H), 3.36 (s, 3H), 3.25 (s, 3H).

6,7-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A304”)

HPLC/MS 1.24 min (A), [M+H]⁺ 450;

¹H NMR (500 MHz, DMSO-d₆) δ 12.20 (s, 1H), 9.16 (s, 1H), 8.43 (s, 1H),8.39 (s, 1H), 8.06-7.91 (m, 2H), 7.74 (dd, J=10.8, 8.4 Hz, 1H),7.60-7.49 (m, 2H), 7.29 (dd, J=11.4, 7.1 Hz, 1H), 3.70-3.31 (m, 4H),2.45-2.25 (m, 4H), 2.21 (s, 3H).

6-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one(“A305”)

UPLC/MS 0.50 min, [M+H]⁺ 448;

¹H NMR (500 MHz, DMSO-d₆) δ 12.13 (bs, 1H), 9.18 (s, 1H), 8.45 (s, 1H),8.40 (s, 1H), 7.99-7.93 (m, 2H), 7.74 (d, J=2.4 Hz, 1H), 7.59-7.55 (m,2H), 7.53 (dd, J=8.7, 2.4 Hz, 1H), 7.37 (d, J=8.8 Hz, 1H), 3.8-3.3 (m,4H), 2.45-2.25 (m, 4H), 2.21 (s, 3H).

Example 203-{1-[4-((S)-3-amino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A306”)

MS [M+H]⁺ 419; HCl salt;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.30 (s, 1H), 9.31(s, 1H), 8.86 (s, 1H), 8.30 (br. s, 2H), 8.18 (br. s, 1H), 8.13 (d,J=8.6 Hz, 2H), 7.88 -7.70 (m, 3H), 7.54-7.39 (m, 2H), 3.97-3.65 (m, 3H),3.66-3.45 (m, 2H), 2.25 (br. s, 1H), 2.06 (br. s, 1H).

The following compounds are prepared similarly:

6,7-difluoro-3-{1-[4-((cis)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A307”)

UPLC/MS 0.47 min, [M+H]⁺ 463;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.29 (s, 1H), 8.86 (s, 1H),8.23-8.09 (m, 2H), 7.98 (dd, J=10.8, 8.5 Hz, 1H), 7.84-7.75 (m, 2H),7.37 (dd, J=11.3, 7.0 Hz, 1H), 3,85-3,05 (m, 1 OH).

6-fluoro-3-{1-[4-((cis)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A308”)

HPLC/MS 1.25 min (A), [M+H]+ 445;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.32 (s, 1H), 8.87 (s, 1H), 8.12 (d,J=8.6 Hz, 2H), 7.79 (d, J=8.6 Hz, 2H), 7.72 (dd, J=9.1, 2.8 Hz, 1H),7.49 (dd, J=9.0, 4.7 Hz, 1H), 7.40 (td, J=8.8, 2.8 Hz, 1H), 3.90-3.04(m, 10H).

3-{1-[4-((R)-3-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-onehydrochloride (“A309”)

UPLC/MS 0.47 min, [M+H]⁺ 451;

¹H NMR (500 MHz, DMSO-d₆) δ 12.36 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.34-8.01 (m, 6H), 7.69 (d, J=8.5 Hz, 2H), 7.36 (dd, J=11.4, 7.0 Hz,1H), 4.47-3.01 (m, 4H), 2.14-2.01 (m, 1H), 1.86-1.49 (m, 4H).

3-{1-[4-((S)-3-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-onehydrochloride (“A310”)

UPLC/MS 0.47 min, [M+H]⁺ 451.

¹H NMR (500 MHz, DMSO-d₆) δ 12.36 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.34-8.01 (m, 6H), 7.69 (d, J=8.5 Hz, 2H), 7.36 (dd, J=11.4, 7.0 Hz,1H), 4.47-3.01 (m, 4H), 2.14-2.01 (m, 1H), 1.86-1.49 (m, 4H).

6-Fluoro-3-{1-[4-((R)-3-methylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-onehydrochloride (“A311”)

MS [M+H]⁺ 433; HCl salt;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.30 (s, 1H), 9.31(s, 1H), 9.27-8.91 (m, 2H, NH₂ ⁺), 8.86 (s, 1H), 8.13 (d, J=8.6 Hz, 2H),7.85-7.74 (m, 3H), 7.51-7.41 (m, 2H), 3.92-3.68 (m, 3H), 3.68-3.51 (m,2H), 2.65 (s, 1.8H), 2.56 (s, 1.2H), 2.27 (br. s, 1H), 2.17 (br. s, 1H).

6-fluoro-3-{1-[4-((S)-3-methylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-onehydrochloride (“A312”)

MS [M+H]+ 433; HCl salt;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.30 (s, 1H), 9.31(s, 1H), 9.27-8.91 (m, 2H, NH₂ ⁺), 8.86 (s, 1H), 8.13 (d, J=8.6 Hz, 2H),7.85-7.74 (m, 3H), 7.51-7.41 (m, 2H), 3.92-3.68 (m, 3H), 3.68-3.51 (m,2H), 2.65 (s, 1.8H), 2.56 (s, 1.2H), 2.27 (br. s, 1H), 2.17 (br. s, 1H).

3-{1-[4-((R)-3-amino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-onehydrochloride (“A313”)

MS [M+H]⁺ 419; HCl salt;

¹H NMR (500 MHz, DMSO-d⁶) mixture of 2 rotamers δ 12.30 (s, 1H), 9.31(s, 1H), 8.86 (s, 1H), 8.30 (br. s, 2H), 8.18 (br. s, 1H), 8.13 (d,J=8.6 Hz, 2H), 7.88 -7.70 (m, 3H), 7.54-7.39 (m, 2H), 3.97-3.65 (m, 3H),3.66-3.45 (m, 2H), 2.25 (br. s, 1H), 2.06 (br. s, 1H).

6-fluoro-3-{1-[4-((R)-3-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-onehydrochloride (“A314”)

MS [M+H]⁺ 449; dihydrochloride;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ ¹H NMR (500 MHz,DMSO-d₆) δ 12.29 (s, 1H), 9.42 (br. s, 1H), 9.30 (s, 1H), 9.10 (br. s,1H), 8.85 (s, 1H), 8.12 (d, J=8.6 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H),7.72 (d, J=8.5 Hz, 2H), 7.50-7.40 (m, 2H), 5.47 (s, 1H), 4.49 (br. s,1H), 3.64 (br. s, 2H), 3.57 (s, 2H), 3.47-3.33 (m, 2H), 3.22-2.95 (m,2H).

6-fluoro-3-{1-[4-((S)-2-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A315”)

MS [M+H]⁺ 449;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.30 (s, 1H), 9.28(s, 1H), 8.86 (s, 1H), 8.07 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz,1H), 7.63 (d, J=8.4 Hz, 2H), 7.50-7.40 (m, 2H), 4.91 (br. s, 1H),4.49-4.04 (m, 1H), 3.93-3.45 (m, 3H), 3.13-2.54 (m, 4H), 2.20-1.95 (m,1H).

6-fluoro-3-{1-[4-((R)-2-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A316”)

MS [M+H]⁺ 449;

¹H NMR (500 MHz, DMSO-d₆) mixture of 2 rotamers δ 12.30 (s, 1H), 9.28(s, 1H), 8.86 (s, 1H), 8.07 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz,1H), 7.63 (d, J=8.4 Hz, 2H), 7.50-7.40 (m, 2H), 4.91 (br. s, 1H),4.49-4.04 (m, 1H), 3.93-3.45 (m, 3H), 3.13-2.54 (m, 4H), 2.20-1.95 (m,1H).

3-{1-[4-(6-amino-3-aza-bicyclo[3.1.0]hexane-3-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A317”)

MS [M+H]⁺ 431;

¹H NMR (400 MHz, DMSO-d₆) δ 12.33 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.07 (d, J=8.7 Hz, 2H), 7.81 (dd, J=9.2, 2.6 Hz, 1H), 7.67 (d, J=8.7 Hz,2H), 7.51 -7.39 (m, 2H), 3.89 (d, J=12.1 Hz, 1H), 3.66 (dd, J=10.6, 4.4Hz, 1H), 3.45 (dd, J=12.0, 4.4 Hz, 1H), 3.38 (d, J=10.7 Hz, 1H), 2.00(t, J=2.2 Hz, 1H), 1.56-1.41 (m, 2H).

6-chloro-3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A318”)

HPLC/MS 1.35 min (A), [M+H]⁺ 477;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.21 (s, 1H), 8.75 (s, 1H),8.11-8.01 (m, 2H), 7.84 (d, J=2.3 Hz, 1H), 7.78-7.72 (m, 2H), 7.43 (dd,J=8.8, 2.3 Hz, 1H), 7.38 (d, J=8.7 Hz, 1H), 4.55 (qd, J=7.7, 3.4 Hz,1H), 3.56 (dt, J=10.3, 7.3 Hz, 1H), 3.50-3.38 (m, 2H), 3.18 (dd, J=13.5,3.5 Hz, 1H), 2.98 (s, 3H), 2.84 (s, 3H), 2.16 (dq, J=13.2, 6.6 Hz, 1H),1.86 (dq, J=11.3, 5.8 Hz, 1H), 1.80-1.61 (m, 2H).

3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A319”)

UPLC/MS 0.50 min, [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.19 (s, 1H), 8.75 (s, 1H), 8.00 (d,J=8.2 Hz, 2H), 7.72 (d, J=8.4 Hz, 2H), 7.55-7.48 (m, 1H), 7.39 (dd,J=9.1, 4.7 Hz, 1H), 7.23 (td, J=8.8, 2.8 Hz, 1H), 4.57-4.47 (m, 1H),3.63-3.49 (m, 1H), 3.49-3.36 (m, 2H), 3.15 (dd, J=13.5, 3.3 Hz, 1H),2.97 (s, 3H), 2.82 (s, 3H), 2.20-2.10 (m, 1H), 1.97-1.79 (m, 1H),1.79-1.58 (m, 2H).

3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A320”)

UPLC/MS 0.52 min, [M+H]⁺ 479;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.17 (s, 1H), 8.74 (s, 1H), 8.01 (d,J=8.6 Hz, 2H), 7.83-7.71 (m, 3H), 7.27 (dd, J=11.4, 7.0 Hz, 1H),4.58-4.48 (m, 1H), 3.63-3.50 (m, 1H), 3.49-3.36 (m, 2H), 3.16 (dd,J=13.4, 3.4 Hz, 1H), 2.20-2.10 (m, 1H), 1.92-1.80 (m, 1H), 1.80-1.57 (m,2H).

3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A321”)

UPLC/MS 0.50 min, [M+H]⁺ 461;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.26 (s, 1H), 8.80 (s, 1H),8.15-8.07 (m, 2H), 7.84-7.76 (m, 2H), 7.64 (dd, J=9.1, 2.8 Hz, 1H), 7.42(dd, J=9.0, 4.7 Hz, 1H), 7.32 (td, J=8.8, 2.8 Hz, 1H), 4.57 (qd, J=7.5,3.7 Hz, 1H), 3.58 (dt, J=10.5, 7.3 Hz, 1H), 3.49-3.41 (m, 2H), 3.20 (dd,J=13.4, 3.8 Hz, 1H), 3.00 (s, 3H), 2.86 (s, 3H), 2.21-2.12 (m, 1H),1.95-1.84 (m, 1H), 1.82-1.64 (m, 2H).

6-chloro-3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A322”)

UPLC/MS 0.53 min, [M+H]⁺ 477;

¹H NMR (500 MHz, DMSO-d₆, TFA-d₁) δ 9.21 (s, 1H), 8.75 (s, 1H),8.11-8.01 (m, 2H), 7.84 (d, J=2.3 Hz, 1H), 7.78-7.72 (m, 2H), 7.43 (dd,J=8.8, 2.3 Hz, 1H), 7.38 (d, J=8.7 Hz, 1H), 4.55 (qd, J=7.7, 3.4 Hz,1H), 3.56 (dt, J=10.3, 7.3 Hz, 1H), 3.50-3.38 (m, 2H), 3.18 (dd, J=13.5,3.5 Hz, 1H), 2.98 (s, 3H), 2.84 (s, 3H), 2.16 (dq, J=13.2, 6.6 Hz, 1H),1.86 (dq, J=11.3, 5.8 Hz, 1H), 1.80-1.61 (m, 2H).

3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A323”)

UPLC/MS 0.51 min, [M+H]⁺ 479;

¹H NMR (400 MHz, DMSO-d₆) δ 12.35 (s, 1H), 9.30 (s, 1H), 9.11 (bs, 1H,NH⁺), 8.86 (s, 1H), 8.19-8.13 (m, 2H), 8.10 (dd, J=11.0, 8.6 Hz, 1H),7.86-7.76 (m, 2H), 7.34 (dd, J=11.4, 7.1 Hz, 1H), 4.64-4.54 (m, 1H),3.64-3.54 (m, 1H), 3.51-3.39 (m, 2H), 3.28-2.16 (m, 1H), 3.08-2.80 (m,6H), 2.22-2.10 (m, 1H), 2.01-1.88 (m, 1H), 1.86-1.68 (m, 2H).

3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A324”)

UPLC/MS 0.51 min, [M+H]⁺ 460;

¹H NMR (400 MHz, DMSO-d₆) δ 12.12 (s, 1H), 9.21 (s, 1H), 9.12 (bs, 1H,NH⁺), 8.48 (s, 1H), 8.42 (s, 1H), 8.10-7.96 (m, 2H), 7.84-7.66 (m, 2H),7.50 (dd, J=8.5, 1.9 Hz, 1H), 7.44-7.30 (m, 2H), 4.63-4.54 (m, 1H),3.66-3.56 (m, 1H), 3.55-3.14 (m, 3H), 3.01 (d, J=4.2 Hz, 3H), 2.88 (d,J=4.2 Hz, 3H), 2.22-2.11 (m, 1H), 2.04-1.87 (m, 1H), 1.85-1.66 (m, 2H).

3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A325”)

UPLC/MS 0.51 min, [M+H]⁺ 460;

¹H NMR (400 MHz, DMSO-d₆) δ 12.12 (s, 1H), 9.21 (s, 1H), 9.12 (bs, 1H,NH⁺), 8.48 (s, 1H), 8.42 (s, 1H), 8.10-7.96 (m, 2H), 7.84-7.66 (m, 2H),7.50 (dd, J=8.5, 1.9 Hz, 1H), 7.44-7.30 (m, 2H), 4.63-4.54 (m, 1H),3.66-3.56 (m, 1H), 3.55-3.14 (m, 3H), 3.01 (d, J=4.2 Hz, 3H), 2.88 (d,J=4.2 Hz, 3H), 2.22-2.11 (m, 1H), 2.04-1.87 (m, 1H), 1.85-1.66 (m, 2H).

Example 213-{1-[4-((S)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A326”)

UPLC/MS 0.46 min, [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.22 (s, 1H), 8.77 (s, 1H),8.11-7.97 (m, 2H), 7.70 (d, J=8.1 Hz, 2H), 7.59 (dd, J=9.2, 2.8 Hz, 1H),7.40 (dd, J=9.0, 4.7 Hz, 1H), 7.28 (td, J=8.8, 2.8 Hz, 1H), 3.87-3.07(m, 6H), 2.87-2.57 (m, 7H), 2.16-2.01 (m, 1H), 1.74-1.59 (m, 1H).

The following compounds are prepared similarly:

6-fluoro-3-{1-[4-((cis)-5-methyl-hexahydro-pyrrolo[3,4-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A327”)

HPLC/MS 1.26 min (A), [M+H]⁺ 459;

¹H NMR (500 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.17 (s, 1H), 8.12-8.04 (m, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.75-7.64(m, 2H), 7.48-7.40 (m, 2H), 3.79 (bs, 1H), 3.67 (bs, 1H), 3.48 (bs, 1H),3.31 (bs, 1H), 2.82 (bs, 2H), 2.52-2.34 (m, 4H), 2.25 (s, 3H).

3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A328”)

HPLC/MS 1.23 min (A), [M+H]⁺ 479;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.12-8.05 (m, 3H), 7.60 (d, J=8.1 Hz, 2H), 7.32 (dd, J=11.4, 7.1 Hz,1H), 4.5-4-2 (m, 1H), 3.77-2.74 (m, 4H), 2.32-2.02 (m, 7H), 1.85-1.62(m, 1H), 1.73 (d, J=36.7 Hz, 1H), 1.54-1.34 (m, 2H).

3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A329”)

HPLC/MS 1.25 min (A), [M+H]⁺ 479;

¹H NMR (400 MHz, DMSO-d₆) δ 12.32 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.12-8.05 (m, 3H), 7.60 (d, J=8.1 Hz, 2H), 7.32 (dd, J=11.4, 7.1 Hz,1H), 4.5-4-2 (m, 1H), 3.77-2.74 (m, 4H), 2.32-2.02 (m, 7H), 1.85-1.62(m, 1H), 1.73 (d, J=36.7 Hz, 1H), 1.54-1.34 (m, 2H).

3-{1-[4-(6-dimethylamino-3-aza-bicyclo[3.1.0]hexane-3-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A330”)

MS [M+H]⁺ 459;

¹H NMR (500 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.28 (s, 1H), 8.85 (s, 1H),8.07 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.7 Hz, 1H), 7.68 (d, J=8.7 Hz,2H), 7.51 -7.37 (m, 2H), 3.90 (d, J=12.1 Hz, 1H), 3.70 (dd, J=10.7, 4.4Hz, 1H), 3.44 (dd, J=12.2, 4.5 Hz, 1H), 3.37 (d, J=10.6 Hz, 1H), 2.21(s, 6H), 1.70-1.57 (m, 2H), 1.35 (t, J=2.1 Hz, 1H).

3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A331”)

HPLC/MS 1.21 min (A), [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.09 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.61 (d, J=8.1 Hz,2H), 7.53 -7.39 (m, 2H), 4.71-0.89 (m, 15H).

3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A332”)

HPLC/MS 1.19 min (A), [M+H]+ 461;

¹H NMR (400 MHz, DMSO-d₆) δ 12.28 (s, 1H), 9.29 (s, 1H), 8.86 (s, 1H),8.09 (d, J=8.4 Hz, 2H), 7.81 (dd, J=9.3, 2.7 Hz, 1H), 7.61 (d, J=8.1 Hz,2H), 7.53 -7.39 (m, 2H), 4.71-0.89 (m, 15H).

3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-fluoro-1H-quinolin-2-one(“A333”)

UPLC/MS 0.46 min, [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.24 (s, 1H), 8.86 (s, 1H),8.08 (d, J=8.2 Hz, 2H), 8.00 (dd, J=9.6, 6.1 Hz, 1H), 7.60 (d, J=8.1 Hz,2H), 7.27 -6.99 (m, 2H), 4.71-0.89 (m, 15H).

3-{1-[4-((R)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A334”)

UPLC/MS 0.46 min, [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.22 (s, 1H), 8.77 (s, 1H),8.11-7.97 (m, 2H), 7.70 (d, J=8.1 Hz, 2H), 7.59 (dd, J=9.2, 2.8 Hz, 1H),7.40 (dd, J=9.0, 4.7 Hz, 1H), 7.28 (td, J=8.8, 2.8 Hz, 1H), 3.87-3.07(m, 6H), 2.87-2.57 (m, 7H), 2.16-2.01 (m, 1H), 1.74-1.59 (m, 1H).

3-{1-[4-((R)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one(“A335”)

UPLC/MS 0.48 min, [M+H]⁺ 479;

¹H NMR (400 MHz, DMSO-d₆, TFA-d₁) δ 9.18 (s, 1H), 8.75 (s, 1H),8.07-7.96 (m, 2H), 7.80 (dd, J=10.8, 8.4 Hz, 1H), 7.69 (d, J=8.1 Hz,2H), 7.28 (dd, J=11.4, 7.0 Hz, 1H), 3.87-3.07 (m, 6H), 2.87-2.57 (m,7H), 2.16-2.01 (m, 1H), 1.74-1.59 (m, 1H).

3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-fluoro-1H-quinolin-2-one(“A336”)

UPLC/MS 0.48 min, [M+H]⁺ 461;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.24 (s, 1H), 8.86 (s, 1H),8.08 (d, J=8.2 Hz, 2H), 8.00 (dd, J=9.6, 6.1 Hz, 1H), 7.60 (d, J=8.1 Hz,2H), 7.27 -6.99 (m, 2H), 4.71-0.89 (m, 15H).

3-{1-[4-((S)-3-diethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A337”)

HPLC/MS 1.25 min (A), [M+H]⁺ 489;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (d, J=2.5 Hz, 1H), 8.86(s, 1H), 8.10 (d, J=8.0 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.71-7.58(m, 2H), 7.55-7.33 (m, 2H), 4.60-4.35 (m, 1H), 3.62-3.46 (m, 1H),3.08-2.90 (m, 1H), 2.78-2.34 (m, 6H), 2.03-1.38 (m, 4H), 0.94 (d, J=69.7Hz, 6H).

3-{1-[4-((R)-3-diethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A338”)

HPLC/MS 1.24 min (A), [M+H]⁺ 489;

¹H NMR (500 MHz, DMSO-d₆) δ 12.29 (s, 1H), 9.30 (d, J=2.5 Hz, 1H), 8.86(s, 1H), 8.10 (d, J=8.0 Hz, 2H), 7.81 (dd, J=9.2, 2.7 Hz, 1H), 7.71-7.58(m, 2H), 7.55-7.33 (m, 2H), 4.60-4.35 (m, 1H), 3.62-3.46 (m, 1H),3.08-2.90 (m, 1H), 2.78-2.34 (m, 6H), 2.03-1.38 (m, 4H), 0.94 (d, J=69.7Hz, 6H).

3-{1-[4-(4-dimethylamino-3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A339”)

HPLC/MS 1.27 min (A), [M+H]⁺ 483;

¹H NMR (700 MHz, DMSO-d₆) 1:1 mixture of rotamers, δ 12.31 (s, 1H), 9.32(s, 1H), 8.87 (s, 1H), 8.12 (d, J=8.3 Hz, 2H), 7.85-7.78 (m, 3H), 7.47(td, J=8.7, 2.8 Hz, 1H), 7.43 (dd, J=9.1, 4.8 Hz, 1H), 4.21-3.78 (m,3H), 3.68 (t, J=10.1 Hz, 0.5H), 3.47 (t, J=10.9 Hz, 0.5H), 3.23 (dq,J=17.7, 9.0 Hz, 1H), 2.33 (s, 3H), 2.24 (s, 3H).

3-{1-[4-((S)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A340”)

UPLC/MS 0.48 min, [M+H]⁺ 460;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers, selection of signalsδ 12.16 (s, 1H), 9.20 (s, 1H), 8.47 (s, 1H), 8.43 (s, 1H), 7.99-7.90 (m,2H), 7.78 -7.65 (m, 2H), 7.50 (dd, J=9.0, 2.5 Hz, 1H), 7.45-7.32 (m,2H), 2.18 (s, 3H), 2.08 (s, 3H).

3-{1-[4-((trans)-3-dimethylamino-4-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one(“A341”)

HPLC/MS 1.23 min (A), [M+H]⁺ 465;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers δ 12.32 (s, 1H), 9.32(s, 1H), 8.87 (s, 1H), 8.24-7.95 (m, 2H), 7.86-7.76 (m, 3H), 7.47 (td,J=8.8, 2.8 Hz, 1H), 7.43 (dd, J=9.0, 4.9 Hz, 1H), 5.30 (m, 1H),4.04-3.49 (m, 4H), 3.05-2.92 (m, 1H), 2.26 (s, 3H), 2.16 (s, 3H).

Example 226-fluoro-3-[1-(4-methylamino-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one(“A342”) and (R)-tetrahydro-furan-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide(“A343”)

“A342”: MS [M+H]⁺ 336;

¹H NMR (400 MHz, DMSO-d₆) δ 12.22 (s, 1H), 8.98 (s, 1H), 8.80 (s, 1H),7.80-7.74 (m, 1H), 7.69 (d, J=8.8 Hz, 2H), 7.46-7.38 (m, 2H), 6.79 (d,J=8.6 Hz, 2H), 4.07 (br. s, 1H), 2.50 (p, J=1.9 Hz, 3H).

“A343”: MS [M+H]⁺ 434;

¹H NMR (400 MHz, DMSO-d₆) δ 12.26 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.08 (d, J=8.6 Hz, 2H), 7.79 (dd, J=9.3, 2.6 Hz, 1H), 7.58 (d, J=8.6 Hz,2H), 7.49 -7.39 (m, 2H), 4.29 (br. s, 1H), 3.81 (q, J=7.1 Hz, 1H), 3.69(br. s, 1H), 3.25 (s, 3H), 2.01 (br. s, 1H), 1.96-1.80 (m, 2H), 1.73(br. s, 1H).

The following compounds are prepared similarly:

(S)-tetrahydro-furan-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide(“A344”)

MS [M+H]⁺ 434;

¹H NMR (400 MHz, DMSO-d₆) δ 12.26 (s, 1H), 9.26 (s, 1H), 8.84 (s, 1H),8.08 (d, J=8.6 Hz, 2H), 7.79 (dd, J=9.3, 2.6 Hz, 1H), 7.58 (d, J=8.6 Hz,2H), 7.49 -7.39 (m, 2H), 4.29 (br. s, 1H), 3.81 (q, J=7.1 Hz, 1H), 3.69(br. s, 1H), 3.25 (s, 3H), 2.01 (br. s, 1H), 1.96-1.80 (m, 2H), 1.73(br. s, 1H).

tetrahydro-pyran-4-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide(“A345”)

MS [M+H]⁺ 448;

¹H NMR (400 MHz, DMSO-d₆) δ 12.27 (s, 1H), 9.27 (s, 1H), 8.85 (s, 1H),8.09 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz, 1H), 7.59 (d, J=8.5 Hz,2H), 7.50 -7.39 (m, 2H), 3.78 (d, J=11.3 Hz, 2H), 3.23 (s, 3H), 3.11(br. s, 2H), 1.65 (qd, J=12.3, 4.4 Hz, 2H), 1.58-1.43 (m, 2H).

(R)—N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-2-methoxy-N-methyl-propionamide(“A346”)

MS [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H), 9.27 (s, 1H), 8.85 (s, 1H),8.10 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.6 Hz, 1H), 7.59 (d, J=8.7 Hz,2H), 7.50 -7.39 (m, 2H), 3.88 (br. s, 1H), 3.26 (s, 3H), 3.08 (s, 3H),1.16 (br. s, 3H).

(2S,4S)-4-methoxy-pyrrolidine-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide(“A347”)

MS [M+H]⁺ 463; hydrochloride

¹H NMR (700 MHz, DMSO-d₆+CF₃COOD) δ 9.34 (s, 1H), 8.88 (s, 1H), 8.22 (d,J=8.4 Hz, 2H), 7.78 (dd, J=9.1, 2.8 Hz, 1H), 7.73 (d, J=8.3 Hz, 2H),7.50-7.40 (m, 2H), 4.26 (dd, J=10.3, 6.9 Hz, 1H), 3.94 (br. s, 1H),3.48-3.38 (m, 1H), 3.34 (s, 3H), 3.22 (s, 3H), 3.13 (dd, J=12.4, 4.7 Hz,1H), 2.07 (ddd, J=16.0, 10.5, 6.1 Hz, 1H), 1.95-1.84 (m, 1H).

(S)—N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-2-methoxy-N-methyl-propionamide(“A348”)

MS [M+H]⁺ 422;

¹H NMR (400 MHz, DMSO-d₆) δ ¹H NMR (400 MHz, DMSO-d₆) δ 12.24 (s, 1H),9.27 (s, 1H), 8.85 (s, 1H), 8.10 (d, J=8.6 Hz, 2H), 7.80 (dd, J=9.2, 2.6Hz, 1H), 7.59 (d, J=8.7 Hz, 2H), 7.50-7.39 (m, 2H), 3.88 (br. s, 1H),3.26 (s, 3H), 3.08 (s, 3H), 1.16 (br. s, 3H).

1-methyl-piperidine-4-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide(“A349”)

MS [M+H]⁺ 461; hydrochloride

¹H NMR (500 MHz, DMSO-d₆) δ 12.34 (s, 1H), 9.76 (s, 1H), 9.30 (s, 1H),8.86 (s, 1H), 8.15 (d, J=7.5 Hz, 2H), 7.82 (dd, J=9.2, 2.8 Hz, 1H), 7.65(d, J=6.6 Hz, 2H), 7.52-7.41 (m, 2H), 3.35-3.26 (m, 2H), 3.22 (s, 3H),2.82 -2.67 (m, 2H), 2.61 (s, 3H), 2.44 (br. s, 1H), 1.99-1.74 (m, 4H).

Example 236-fluoro-3-{1-[5-((S)-3-methoxy-pyrrolidine-1-carbonyl)-thiophen-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A350”)

UPLC/MS 0.70 min, [M+H]⁺ 440;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers δ 12.30 (s, 1H), 9.35(s, 0.5H), 9.34 (s, 0.5H), 8.85 (s, 1H), 8.42 (d, J=1.4 Hz, 1H), 8.22(d, J=1.5 Hz, 0.5H), 8.19 (d, J=1.5 Hz, 0.5H), 7.82 (dd, J=9.3, 2.8 Hz,1H), 7.46 (td, J=8.8, 2.8 Hz, 1H), 7.42 (dd, J=9.1, 4.9 Hz, 1H),4.20-3.87 (m, 3H), 3.75-3.47 (m, 2H), 3.29 (s, 1.5H), 3.27 (s, 1.5H),2.25-1.90 (m, 2H).

The following compounds are prepared similarly:

6-fluoro-3-{1-[5-((R)-3-methoxy-pyrrolidine-1-carbonyl)-thiophen-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one(“A351”)

UPLC/MS 0.71 min, [M+H]⁺ 440;

¹H NMR (500 MHz, DMSO-d₆) 1:1 mixture of rotamers δ 12.30 (s, 1H), 9.35(s, 0.5H), 9.34 (s, 0.5H), 8.85 (s, 1H), 8.42 (d, J=1.4 Hz, 1H), 8.22(d, J=1.5 Hz, 0.5H), 8.19 (d, J=1.5 Hz, 0.5H), 7.82 (dd, J=9.3, 2.8 Hz,1H), 7.46 (td, J=8.8, 2.8 Hz, 1H), 7.42 (dd, J=9.1, 4.9 Hz, 1H),4.20-3.87 (m, 3H), 3.75-3.47 (m, 2H), 3.29 (s, 1.5H), 3.27 (s, 1.5H),2.25-1.90 (m, 2H).

The following examples relate to medicaments:

Example A: Injection vials

A solution of 100 g of an active ingredient of the formula I and 5 g ofdisodium hydrogenphosphate in 3 l of bidistilled water is adjusted to pH6.5 using 2 N hydrochloric acid, sterile filtered, transferred intoinjection vials, lyophilised under sterile conditions and sealed understerile conditions. Each injection vial contains 5 mg of activeingredient.

Example B: Suppositories

A mixture of 20 g of an active ingredient of the formula I with 100 g ofsoya lecithin and 1400 g of cocoa butter is melted, poured into mouldsand allowed to cool. Each suppository contains 20 mg of activeingredient.

Example C: Solution

A solution is prepared from 1 g of an active ingredient of the formulaI, 9.38 g of NaH₂PO₄-2H₂O, 28.48 g of Na₂HPO₄.12 H₂O and 0.1 g ofbenzalkonium chloride in 940 ml of bidistilled water. The pH is adjustedto 6.8, and the solution is made up to 1 l and sterilised byirradiation. This solution can be used in the form of eye drops.

Example D: Ointment

500 mg of an active ingredient of the formula I are mixed with 99.5 g ofVaseline under aseptic conditions.

Example E: Tablets

A mixture of 1 kg of active ingredient of the formula I, 4 kg oflactose, 1.2 kg of potato starch, 0.2 kg of talc and 0.1 kg of magnesiumstearate is pressed in a conventional manner to give tablets in such away that each tablet contains 10 mg of active ingredient.

Example F: Dragees

Tablets are pressed analogously to Example E and subsequently coated ina conventional manner with a coating of sucrose, potato starch, talc,tragacanth and dye.

Example G: Capsules

2 kg of active ingredient of the formula I are introduced into hardgelatine capsules in a conventional manner in such a way that eachcapsule contains 20 mg of the active ingredient.

Example H: Ampoules

A solution of 1 kg of active ingredient of the formula I in 60 l ofbidistilled water is sterile filtered, transferred into ampoules,lyophilised under sterile conditions and sealed under sterileconditions. Each ampoule contains 10 mg of active ingredient.

1-8. (canceled)
 9. Medicaments comprising at least one compound of theformula I

in which X¹, X², X³, X⁴ each, independently of one another, denote CH orN, Y denotes N or CH, Q denotes H or CH₃, R¹ denotes H, F, Cl, Br, CN,CH₃, CF₃ or OCH₃, R² denotes H, F, or Cl, R³ denotes phenyl, napthyl,pyridyl, pyrimidinyl, quinolinyl, isoquinolinyl, indolyl, indazolyl,thiophenyl, dihydroisoindolyl or benzimidazolyl, each of with isunsubstituted or mono-, di- or trisubstituted by Hal, CN, NO₂, A,(CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)_(n)CON(R⁴)₂,(CR⁴)_(n)COHet, (CR⁴)_(n)SO₂N(R⁴)₂, (CR⁴)_(n)SO₂Het, (CR⁴)_(n)N(R⁴)₂,(CR⁴)_(n)Net, O(CR⁴)_(n)COHet, (CR⁴)_(n)O(CR⁴)_(n)Het,(CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het, (CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het,(CR⁴)_(n)CON(R⁴)(CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)N(R⁴)COA,(CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or (CR⁴)_(n)COOR⁴, R⁴ denotes Hor A′, A denotes unbranched or branched alkyl with 1-10 C-atoms, whereintwo adjacent carbon atoms may form a double bond and/or one or twonon-adjacent CH- and/or CH₂-groups may be replaced by N-, O- and/orS-atoms and wherein 1-7H-atoms may be replaced by R⁵, or cyclic alkylhaving 3-7 C atoms, A′ denotes unbranched or branched alkyl with 1-6C-atoms, wherein one or two non-adjacent CH- and/or CH₂-groups may bereplaced by O-atoms, Cyc denotes cyclobutyl, cyclopentyl or cyclohexyl,each of which is unsubstituted or mono- or disubstituted by A, Hal, OR⁴,N(R⁴)₂, Het′, (CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂ and/or ═O, R⁵ denotes F,Cl or OH, Het denotes pyrrolidinyl, morpholinyl, piperidinyl,piperazinyl, [1,4]-diazepanyl, oxazolidinyl,hexahydro-pyrrolo[3,4-c]pyrrolyl, 2-oxa-6-aza-spiro[3,4]octanyl,2-oxa-6-aza-spiro[3,5]nonanyl, 2-oxa-7-aza-spiro[3,5]nonanyl,2,5-dioxa-8-aza-spiro[3,5]nonanyl, oxetanyl,2-oxa-5-aza-spiro[3,4]octanyl, 2-oxa-6-aza-spiro[3,3]heptanyl,3-aza-bicyclo[3.1.0]hexanyl, 2-oxa-7-aza-spiro[3,5]nonanyl,isoxazolidinyl, azetidinyl, 2,6-diaza-spiro[3,4]octanyl,hexahydro-pyrrolo[3,4-b]pyrrolyl, tetrahydrofuranyl or isothiazolidinyl,each of which is unsubstituted or mono-, di- or trisubstituted by A,Hal, OR⁴, OCOA, COA, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)Het′,(CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂, COHet′, (CR₄)_(n)S(O)_(m)R⁴, and/or═, Het′ denotes pyrrolidinyl, morpholinyl, piperidinyl, oxetanyl,tetrahydrofuranyl, tetrahydropyranyl, pyridyl, pyrazolyl, orpiperazinyl, each of which is unsubstituted or mono- or disubstituted byA, Hal, OR⁴, N(R⁴)₂ and/or ═O, Hal denotes F, Cl, Br or I, n denotes 0,1, 2 or 3, m denotes 0, 1 or 2, with the proviso that only one or two ofX¹, X², X³, X⁴ denote N, and/or pharmaceutically acceptable salts,solvates, tautomers and stereoisomers thereof, including mixturesthereof in all ratios, and optionally a pharmaceutically acceptablecarrier, excipient or vehicle 10-11. (canceled)
 12. The medicaments ofclaim 9 further comprising at least one further medicament activeingredient.
 13. (canceled)
 14. The medicaments of claim 9, where R¹denotes H, F, Cl, Br, CN, CH₃, CF₃ or OCH₃, R² denotes H or F, andpharmaceutically acceptable solvates, salts, tautomers and stereoisomersthereof, including mixtures thereof in all ratios.
 15. The medicamentsof claim 9, wherein R³ denotes phenyl, pyridyl, pyrimidinyl, indolyl,indazolyl, thiophenyl, dihydroisoindolyl or benzimidazolyl, each ofwhich is unsubstituted or mono-, di- or trisubstituted by Hal, A,(CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)CON(R⁴)₂,(CR⁴)_(n)COHet, (CR⁴)_(n)SO₂Het, (CR⁴)_(n)Het, O(CR⁴)_(n)COHet,(CR⁴)_(n)O(CR⁴)Het, (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het,(CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het, (CR⁴)CON(R⁴)(CR⁴)_(n)N(R⁴)₂,(CR⁴)_(n)N(R⁴)COA, (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or(CR⁴)_(n)COOR⁴, and pharmaceutically acceptable salts, tautomers andstereoisomers thereof, including mixtures thereof in all ratios.
 16. Themedicaments of claim 9, wherein A denotes unbranched or branched alkylwith 1-10 C-atoms, wherein two adjacent carbon atoms may form a doublebond and/or one or two non-adjacent CH- and/or CH₂-groups may bereplaced by N- and/or O-atoms and wherein 1-7H-atoms may be replaced byR⁵, and pharmaceutically acceptable salts, tautomers and stereoisomersthereof, including mixtures thereof in all ratios.
 17. The medicamentsof claim 9, wherein Het′ denotes pyrrolidinyl, and pharmaceuticallyacceptable salts, tautomers and stereoisomers thereof, includingmixtures thereof in all ratios.
 18. The medicaments of claim 9, whereinX¹, X², X³, X⁴ each, independently of one another, denote CH or N, Ydenotes N or CH, Q denotes H or CH₃, R¹ denotes H, F, Cl, Br, CN, CH₃,CF₃ or OCH₃, R² denotes H or F, R³ denotes phenyl, pyridyl, pyrimidinyl,indolyl, indazolyl, thiophenyl, dihydroisoindolyl or benzimidazolyl,each of which is unsubstituted or mono-, di- or trisubstituted by Hal,A, (CR⁴)_(n)OR⁴, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)S(O)_(m)R⁴, (CR⁴)CON(R⁴)₂,(CR⁴)_(n)COHet, (CR⁴)_(n)SO₂Het, (CR⁴)_(n)Het, O(CR⁴)_(n)COHet,(CR⁴)_(n)O(CR⁴)Het, (CR⁴)_(n)N(R⁴)(CR⁴)_(n)Het,(CR⁴)_(n)CON(R⁴)(CR⁴)_(n)Het, (CR⁴)CON(R⁴)(CR⁴)_(n)N(R⁴)₂,(CR⁴)_(n)N(R⁴)COA, (CR⁴)_(n)N(R⁴)COHet′, (CR⁴)_(n)OCyc and/or(CR⁴)_(n)COOR⁴, R⁴ denotes H or A′, A denotes unbranched or branchedalkyl with 1-10 C-atoms, wherein two adjacent carbon atoms may form adouble bond and/or one or two non-adjacent CH- and/or CH₂-groups may bereplaced by N- and/or O-atoms and wherein 1-7H-atoms may be replaced byR⁵, Cyc denotes cyclobutyl, cyclopentyl or cyclohexyl, each of which isunsubstituted or mono- or disubstituted by A, Hal, OR⁴, N(R⁴)₂, Het′,(CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂ and/or ═O, A′ denotes unbranched orbranched alkyl with 1-6 C-atoms, wherein one or two non-adjacent CH-and/or CH₂-groups may be replaced by O-atoms, R⁵ denotes F, Cl or OH,Het denotes pyrrolidinyl, morpholinyl, piperidinyl, piperazinyl,[1,4]-diazepanyl, oxazolidinyl, hexahydro-pyrrolo[3,4-c]pyrrolyl,2-oxa-6-aza-spiro[3.4]octanyl, 2-oxa-6-aza-spiro[3.5]nonanyl,2-oxa-7-aza-spiro[3.5]nonanyl, 2,5-dioxa-8-aza-spiro[3.5]nonanyl,oxetanyl, 2-oxa-5-aza-spiro[3.4]octanyl, 2-oxa-6-aza-spiro[3.3]heptanyl,3-aza-bicyclo[3.1.0]hexanyl, 2-oxa-7-aza-spiro[3.5]nonanyl,isoxazolidinyl, azetidinyl, 2,6-diaza-spiro[3.4]octanyl,hexahydro-pyrrolo[3,4-b]pyrrolyl, tetrahydrofuranyl or isothiazolidinyl,each of which is unsubstituted or mono-, di- or trisubstituted by A,Hal, OR⁴, OCOA, COA, (CR⁴)_(n)N(R⁴)₂, (CR⁴)_(n)Het′,(CR⁴)_(n)O(CR⁴)_(n)Het′, CON(R⁴)₂, COHet′, (CR⁴)_(n)S(O)_(m)R⁴, and/or═O, Het′ denotes pyrrolidinyl, oxetanyl, tetrahydrofuranyl,tetrahydropyranyl, pyridyl or pyrazolyl, Hal denotes F, Cl, Br or I, Ndenotes 0, 1, 2 or 3, m denotes 0, 1 or 2, and pharmaceuticallyacceptable salts, tautomers and stereoisomers thereof, includingmixtures thereof in all ratios.
 19. The medicaments of claim 9, selectedfrom the group consisting of6-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-[1-(4-dimethylaminomethyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,8]naphthyridin-2-one,3-(1-phenyl-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one,3-[1-(4-hydroxymethyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,8]naphthyridin-2-one,N-(2-hydroxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,N-(2-methoxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,4-[4-(6-chloro-2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide,3-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-[1-(2-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-{1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N-(1-methyl-piperidin-4-ylmethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,4-[4-(6-methoxy-2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide,4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-pyridine-2-carboxylicacid methyl ester,4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N,N-dimethyl-benzamide,N-(2-hydroxy-ethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-[1-(1H-indol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,N-(2-morpholin-4-yl-ethyl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(1-methyl-piperidin-4-ylmethyl)-benzamide,3-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoic acidmethyl ester,3-[1-(3-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-{1-[4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-(1-phenyl-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,3-[1-(3H-benzimidazol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one,7-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,6-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,3-{1-[3-fluoro-4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[3-fluoro-4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[6-(3-oxo-morpholin-4-yl)-pyridin-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[2-methyl-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(1-hydroxy-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[3-fluoro-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-[1-(3,4,5-trimethoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,2-fluoro-N-methyl-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-{1-[3-methyl-4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,6]naphthyridin-2-one,N,N-dimethyl-4-[4-(2-oxo-1,2-dihydro-[1,7]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,8]naphthyridin-2-one,3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,7]naphthyridin-2-one,3-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-[1,6]naphthyridin-2-one,3-(1-phenyl-1H-pyrazol-4-yl)-1H-[1,6]naphthyridin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,5-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(3-oxo-morpholin-4-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one,3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,4-[4-(2-oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-N-piperidin-4-yl-benzamide,3-[1-(4-piperazin-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,6-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-[1-(2-piperazin-1-yl-pyrimidin-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-[1-(4-[1,4]diazepan-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N-(1-Methyl-piperidin-4-yl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,N-methyl-N-(1-methyl-piperidin-4-yl)-4-[4-(2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,3-{1-[4-(1-methyl-piperidin-4-ylmethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,6]naphthyridin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,7]naphthyridin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,7-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,3-{1-[2-(4-methyl-piperazin-1-yl)-pyrimidin-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(4-methyl-[1,4]diazepan-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,3-(1-phenyl-1H-pyrazol-4-yl)-1H-quinolin-2-one,3-{1-[3-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,4-[4-(2-Oxo-1,2-dihydro-[1,8]naphthyridin-3-yl)-[1,2,3]triazol-1-yl]-benzoicacid,3-{1-[3-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[3-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-[1-(4-isopropenyl-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-{1-[4-(1-methanesulfonyl-1-methyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-chloro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-fluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,5]naphthyridin-2-one,6-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,5-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one,3-(1-{4-[4-(3-methoxy-propyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one,5,7-difluoro-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-bromo-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-methoxy-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-{1-[4-(Morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-8H-pyrido[2,3-d]pyrimidin-7-one,6-fluoro-3-{1-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5,7-difluoro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-chloro-3-{1-[4-(4-methyl-3-oxo-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxo-oxazolidin-3-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(1,1-dioxo-116-isothiazolidin-2-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-(1-{4-[2-(4-acetyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-6-fluoro-1H-quinolin-2-one,3-(1-{4-[2-(4-acetyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-6,7-difluoro-1H-quinolin-2-one,acetic acid1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-piperidin-4-ylester, acetic acid1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1l-yl]-benzoyl}-piperidin-3-ylester,3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-5,7-difluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-(3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[3-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[3-([1,3′]bipyrrolidinyl-1′-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-5-oxo-[1,4]diazepane-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(2-dimethylamino-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-(2-diethylamino-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,7-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,8-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,6-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,6-chloro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-[1-(4-[1,4]diazepan-1-yl-phenyl)-1H-[1,2,3]triazol-4-yl]-6-fluoro-1H-[1,8]naphthyridin-2-one,6-fluoro-3-{1-[3-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-chloro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5,6-difluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(piperazine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(3-piperazin-1-yl-propoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-piperidin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(2-piperidin-4-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(3-piperazin-1-yl-propoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-methyl-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(2-oxo-2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxo-2-piperazin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-trifluoromethyl-1H-quinolin-2-one,3-{1-[4-(4-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-(4-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[1-(2-oxo-2-piperazin-1-yl-ethyl)-1H-indazol-5-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-7-methoxy-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-7-fluoro-3-{1-[4-(piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,8-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,5,7-difluoro-3-{-1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-Fluoro-3-{1-[3-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,7-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-[1,4]diazepan-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-[1,8]naphthyridin-2-one,5,6-difluoro-3-{-1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-piperazine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-(1-methyl-piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[2-(1-methyl-piperidin-4-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(1-methyl-piperidine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[2-(1-methyl-piperidin-4-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-trifluoromethyl-1H-quinolin-2-one,3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-(4-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6,7-difluoro-3-(1-{1-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-1H-indazol-5-yl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(4-methyl-2-oxo-piperazin-1-yl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-Fluoro-3-(1-{4-[4-(2-methoxy-ethyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-[1,8]naphthyridin-2-one,6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-yl)-ethoxy]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-2-oxo-1,2-dihydro-quinoline-7-carbonitrile,6-fluoro-3-(1-{1-[2-(4-methyl-piperazin-1-yl)-2-oxo-ethyl]-1H-indol-5-yl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,acetic acid(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1l-yl]-benzoyl}-pyrrolidin-3-ylester, acetic acid(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidin-3-ylester,6-fluoro-3-{1-[4-((R)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-hydroxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-hydroxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(3-hydroxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,4-methyl-3-{1-[4-(morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-Difluoro-3-{1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N-(2-diethylamino-ethyl)-4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,4-[4-(7-chloro-6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-diethylamino-ethyl)-benzamide,3-(1-{4-[4-(2-diethylamino-ethyl)-piperazine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-6,7-difluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(4-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((R)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((S)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methoxy-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N-(2-diethylamino-ethyl)-4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,6-fluoro-3-{1-[4-((S)-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((R)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((S)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-(1-{4-[3-(2-diethylamino-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-7-aza-spiro[4.4]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-6-aza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(3-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(3-dimethylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-(1-{4-[3-(4-hydroxy-piperidin-1-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[3-(2-morpholin-4-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-methoxy-ethyl)-N-methyl-benzamide,4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-(2-methoxy-ethyl)-N-methyl-benzamide,6-fluoro-3-{1-[4-((R)-3-hydroxymethyl-morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-hydroxymethyl-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-hydroxymethyl-morpholine-4-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((2S,5S)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((2R,5R)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((2S,5S)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-((2R,5R)-2,5-bis-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[3-(2-morpholin-4-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-7-methyl-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[3-(2-pyrrolidin-1-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6,7-difluoro-3-(1-{4-[3-(2-pyrrolidin-1-yl-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}I-pyrrolidine-3-carboxylicacid amide,6-fluoro-3-{1-[4-((2S,4R)-4-hydroxy-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}1-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-6-aza-spiro[3.5]nonane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-7-aza-spiro[3.5]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-oxetan-3-yl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}1-1H-quinolin-2-one,3-{1-[4-(2,5-dioxa-8-aza-spiro[3.5]nonane-8-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N-oxetan-3-yl-benzamide,6,7-difluoro-3-(1-1{4-[(S)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-5-aza-spiro[30.4]octane-5-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[14-(2-oxa-6-aza-spiro[3.3]heptane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-1-{4-[(S)-3-(2-methoxy-ethoxymethyl)-pyrrolidine-1-carbonyl]-phenyl}1-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,3-{1-[4-((3R,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-N,N-bis-(2-methoxy-ethyl)-benzamide,3-{1-[4-(3-diethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,N-(3-acetyl-3-aza-bicyclo[3.1.0]hex-6-yl)-4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzamide,6-fluoro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-2-carboxylicacid amide,(S)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-3-carboxylicacid amide,6-fluoro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-oxa-5-aza-spiro[3.5]nonane-5-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-2-hydroxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-(1-{4-[3-(4-hydroxy-piperidin-1-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-chloro-3-{1-[1-(4-(4-oxetan-3-yl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(3-dimethylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(2-hydroxymethyl-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(2-oxa-7-aza-spiro[3.5]nonane-7-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(2-oxa-6-aza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(2-oxa-6-aza-spiro[3.3]heptane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-chloro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-(1-{4-[(R)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-pyrazol-4-yl)-1H-quinolin-2-one,(R)-1-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-benzoyl}-pyrrolidine-2-carboxylicacid amide,3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-chloro-3-{1-[4-(3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-3-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{-1-[4-((S)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-4-hydroxy-isoxazolidine-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-2-pyrrolidin-1-ylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-2-pyrrolidin-1-ylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(azetidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-(1-{4-[2-(4-methyl-piperazine-1-carbonyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methanesulfonyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methanesulfonyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(3-methanesulfonylmethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-{4-[2-(1-methyl-1H-pyrazol-4-yl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-pyridin-3-yl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-{4-[2-(4-methyl-piperazin-1-ylmethyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(2-methyl-2,6-diaza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(2-methyl-2,6-diaza-spiro[3.4]octane-6-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((3aR,6aR)-5-methyl-hexahydro-pyrrolo[3,4-b]pyrrole-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(2,2-dimethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-(1-{4-[3-(4-methyl-piperazine-1-carbonyl)-pyrrolidine-1-carbonyl]-phenyl}-1H-[1,2,3]triazol-4-yl)-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-2-methyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-(1-{4-[(S)-3-(2-methoxy-ethoxy)-pyrrolidine-1-carbonyl]-phenyl}-1H-pyrazol-4-yl)-1H-quinolin-2-one,3-{1-[4-((3R,4R)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-((2S,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((2R,4R)-2-hydroxymethyl-4-methoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((3S,4S)-3,4-dimethoxy-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(4-methyl-piperazine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((S)-3-amino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((cis)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((cis)-hexahydro-pyrrolo[3,4pyrrole-2-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((R)-3-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{-1-[4-((S)-3-amino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,6-Fluoro-3-{1-[4-((R)-3-methylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methylamino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((R)-3-amino-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-2-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-2-hydroxymethyl-piperazine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-(6-amino-3-aza-bicyclo[3.1.0]hexane-3-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-((S)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-2-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-((cis)-5-methyl-hexahydro-pyrrolo[3,4-c]pyrrole-2-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-(6-dimethylamino-3-aza-bicyclo[3.1.0]hexane-3-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6,7-difluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-dimethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-7-fluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-diethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((R)-3-diethylamino-piperidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-(4-dimethylamino-3,3-difluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((S)-3-dimethylaminomethyl-pyrrolidine-1-carbonyl)-phenyl]-1H-pyrazol-4-yl}-6-fluoro-1H-quinolin-2-one,3-{1-[4-((trans)-3-dimethylamino-4-fluoro-pyrrolidine-1-carbonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-6-fluoro-1H-quinolin-2-one,6-fluoro-3-[1-(4-methylamino-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,(R)-tetrahydro-furan-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide,(S)-tetrahydro-furan-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide,tetrahydro-pyran-4-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide,(R)—N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-2-methoxy-N-methyl-propionamide,(2S,4S)-4-methoxy-pyrrolidine-2-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide,(S)—N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-2-methoxy-N-methyl-propionamide,1-methyl-piperidine-4-carboxylic acid{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-methyl-amide,6-fluoro-3-{1-[5-((S)-3-methoxy-pyrrolidine-1-carbonyl)-thiophen-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[5-((R)-3-methoxy-pyrrolidine-1-carbonyl)-thiophen-3-yl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,N-{4-[4-(6,7-difluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-N-methyl-acetamide,N-{4-[4-(6-fluoro-2-oxo-1,2-dihydro-quinolin-3-yl)-[1,2,3]triazol-1-yl]-phenyl}-N-methyl-acetamide,6-fluoro-3-[1-(2-methyl-1-oxo-2,3-dihydro-1H-isoindol-5-yl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,6-Fluoro-3-{1-[4-((trans)-3-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[1-(4-((1S,3R)-3-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-3-methoxy-pyrrolidine-1-sulfonyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((1S,2S)-2-methoxy-cyclopentyloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-[1-(4-cyclopentyloxy-phenyl)-1H-[1,2,3]triazol-4-yl]-1H-quinolin-2-one,3-[1-(4-cyclopentyloxy-phenyl)-1H-[1,2,3]triazol-4-yl]-6-fluoro-1H-quinolin-2-one,6-fluoro-3-{1-[4-(tetrahydro-furan-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(tetrahydro-furan-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(1-methyl-piperidin-4-ylmethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((S)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6,7-difluoro-3-{1-[4-((R)-1-methyl-pyrrolidin-3-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(1-methyl-piperidin-4-ylmethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-fluoro-3-{1-[4-(1-methyl-piperidin-4-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,6-chloro-3-{1-[4-(1-methyl-piperidin-4-yloxy)-phenyl]-1H-[1,2,3]triazol-4-yl}-1H-quinolin-2-one,and pharmaceutically acceptable solvates, salts, tautomers andstereoisomers thereof, including mixtures thereof in all ratios.